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17
en
Naloxone reverses the antihypertensive effect of clonidine .
[ { "start": 0, "end": 8, "label": "Chemical", "value": "Naloxone" }, { "start": 49, "end": 58, "label": "Chemical", "value": "clonidine" } ]
en
In unanesthetized , spontaneously hypertensive rats the decrease in blood pressure and heart rate produced by intravenous clonidine , 5 to 20 micrograms / kg , was inhibited or reversed by nalozone , 0 .
[ { "start": 34, "end": 46, "label": "Disease", "value": "hypertensive" }, { "start": 122, "end": 131, "label": "Chemical", "value": "clonidine" }, { "start": 189, "end": 197, "label": "Chemical", "value": "nalozone" } ]
en
2 to 2 mg / kg .
[]
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The hypotensive effect of 100 mg / kg alpha-methyldopa was also partially reversed by naloxone .
[ { "start": 4, "end": 15, "label": "Disease", "value": "hypotensive" }, { "start": 38, "end": 54, "label": "Chemical", "value": "alpha-methyldopa" }, { "start": 86, "end": 94, "label": "Chemical", "value": "naloxone" } ]
en
Naloxone alone did not affect either blood pressure or heart rate .
[ { "start": 0, "end": 8, "label": "Chemical", "value": "Naloxone" } ]
en
In brain membranes from spontaneously hypertensive rats clonidine , 10 (- 8 ) to 10 (- 5 ) M , did not influence stereoselective binding of [3H]-naloxone ( 8 nM ), and naloxone , 10 (- 8 ) to 10 (- 4 ) M , did not influence clonidine - suppressible binding of [3H]-dihydroergocryptine ( 1 nM ). These findings indicate t...
[ { "start": 38, "end": 50, "label": "Disease", "value": "hypertensive" }, { "start": 56, "end": 65, "label": "Chemical", "value": "clonidine" }, { "start": 140, "end": 153, "label": "Chemical", "value": "[3H]-naloxone" }, { "start": 168, "end": 176,...
en
As naloxone and clonidine do not appear to interact with the same receptor site , the observed functional antagonism suggests the release of an endogenous opiate by clonidine or alpha-methyldopa
[ { "start": 3, "end": 11, "label": "Chemical", "value": "naloxone" }, { "start": 16, "end": 25, "label": "Chemical", "value": "clonidine" }, { "start": 165, "end": 174, "label": "Chemical", "value": "clonidine" }, { "start": 178, "end": 194, "la...
en
Lidocaine - induced cardiac asystole .
[ { "start": 0, "end": 9, "label": "Chemical", "value": "Lidocaine" }, { "start": 20, "end": 36, "label": "Disease", "value": "cardiac asystole" } ]
en
Intravenous administration of a single 50 - mg bolus of lidocaine in a 67 - year - old man resulted in profound depression of the activity of the sinoatrial and atrioventricular nodal pacemakers .
[ { "start": 56, "end": 65, "label": "Chemical", "value": "lidocaine" }, { "start": 112, "end": 122, "label": "Disease", "value": "depression" } ]
en
The patient had no apparent associated conditions which might have predisposed him to the development of bradyarrhythmias ; and , thus , this probably represented a true idiosyncrasy to lidocaine
[ { "start": 105, "end": 121, "label": "Disease", "value": "bradyarrhythmias" }, { "start": 186, "end": 195, "label": "Chemical", "value": "lidocaine" } ]
en
Suxamethonium infusion rate and observed fasciculations .
[ { "start": 0, "end": 13, "label": "Chemical", "value": "Suxamethonium" }, { "start": 41, "end": 55, "label": "Disease", "value": "fasciculations" } ]
en
A dose - response study .
[]
en
Suxamethonium chloride ( Sch ) was administered i .
[ { "start": 0, "end": 22, "label": "Chemical", "value": "Suxamethonium chloride" }, { "start": 25, "end": 28, "label": "Chemical", "value": "Sch" } ]
en
v .
[]
en
to 36 adult males at six rates : 0 .
[]
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25 mg s - 1 to 20 mg s - 1 .
[]
en
The infusion was discontinued either when there was no muscular response to tetanic stimulation of the ulnar nerve or when Sch 120 mg was exceeded .
[ { "start": 76, "end": 83, "label": "Disease", "value": "tetanic" }, { "start": 123, "end": 126, "label": "Chemical", "value": "Sch" } ]
en
Six additional patients received a 30 - mg i .
[]
en
v .
[]
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bolus dose .
[]
en
Fasciculations in six areas of the body were scored from 0 to 3 and summated as a total fasciculation score .
[ { "start": 0, "end": 14, "label": "Disease", "value": "Fasciculations" }, { "start": 88, "end": 101, "label": "Disease", "value": "fasciculation" } ]
en
The times to first fasciculation , twitch suppression and tetanus suppression were inversely related to the infusion rates .
[ { "start": 19, "end": 32, "label": "Disease", "value": "fasciculation" }, { "start": 35, "end": 41, "label": "Disease", "value": "twitch" }, { "start": 58, "end": 65, "label": "Disease", "value": "tetanus" } ]
en
Fasciculations in the six areas and the total fasciculation score were related directly to the rate of infusion .
[ { "start": 0, "end": 14, "label": "Disease", "value": "Fasciculations" }, { "start": 46, "end": 59, "label": "Disease", "value": "fasciculation" } ]
en
Total fasciculation
[ { "start": 6, "end": 19, "label": "Disease", "value": "fasciculation" } ]
en
Galanthamine hydrobromide , a longer acting anticholinesterase drug , in the treatment of the central effects of scopolamine ( Hyoscine ). Galanthamine hydrobromide , an anticholinesterase drug capable of penetrating the blood - brain barrier , was used in a patient demonstrating central effects of scopolamine ( hyosci...
[ { "start": 0, "end": 25, "label": "Chemical", "value": "Galanthamine hydrobromide" }, { "start": 113, "end": 124, "label": "Chemical", "value": "scopolamine" }, { "start": 127, "end": 135, "label": "Chemical", "value": "Hyoscine" }, { "start": 139, ...
en
It is longer acting than physostigmine and is used in anaesthesia to reverse the non - depolarizing neuromuscular block .
[ { "start": 25, "end": 38, "label": "Chemical", "value": "physostigmine" } ]
en
However , studies into the dose necessary to combating scopolamine
[ { "start": 55, "end": 66, "label": "Chemical", "value": "scopolamine" } ]
en
Effects of uninephrectomy and high protein feeding on lithium - induced chronic renal failure in rats .
[ { "start": 54, "end": 61, "label": "Chemical", "value": "lithium" }, { "start": 72, "end": 93, "label": "Disease", "value": "chronic renal failure" } ]
en
Rats with lithium - induced nephropathy were subjected to high protein ( HP ) feeding , uninephrectomy ( NX ) or a combination of these , in an attempt to induce glomerular hyperfiltration and further progression of renal failure .
[ { "start": 10, "end": 17, "label": "Chemical", "value": "lithium" }, { "start": 28, "end": 39, "label": "Disease", "value": "nephropathy" }, { "start": 216, "end": 229, "label": "Disease", "value": "renal failure" } ]
en
Newborn female Wistar rats were fed a lithium - containing diet ( 50 mmol / kg ) for 8 weeks and then randomized to normal diet , HP diet ( 40 vs .
[ { "start": 38, "end": 45, "label": "Chemical", "value": "lithium" } ]
en
19 %), NX or HP + NX for another 8 weeks .
[]
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Corresponding non - lithium pretreated groups were generated .
[ { "start": 20, "end": 27, "label": "Chemical", "value": "lithium" } ]
en
When comparing all lithium treated versus non - lithium - treated groups , lithium caused a reduction in glomerular filtration rate ( GFR ) without significant changes in effective renal plasma flow ( as determined by a marker secreted into the proximal tubules ) or lithium clearance .
[ { "start": 19, "end": 26, "label": "Chemical", "value": "lithium" }, { "start": 48, "end": 55, "label": "Chemical", "value": "lithium" }, { "start": 75, "end": 82, "label": "Chemical", "value": "lithium" }, { "start": 267, "end": 274, "label": ...
en
Consequently , lithium pretreatment caused a fall in filtration fraction and an increase in fractional Li excretion .
[ { "start": 15, "end": 22, "label": "Chemical", "value": "lithium" }, { "start": 103, "end": 105, "label": "Chemical", "value": "Li" } ]
en
Lithium also caused proteinuria and systolic hypertension in absence of glomerulosclerosis .
[ { "start": 0, "end": 7, "label": "Chemical", "value": "Lithium" }, { "start": 20, "end": 31, "label": "Disease", "value": "proteinuria" }, { "start": 45, "end": 57, "label": "Disease", "value": "hypertension" }, { "start": 72, "end": 90, "label...
en
HP failed to accentuante progression of renal failure and in fact tended to increase GFR and decrease plasma creatinine levels in lithium pretreated rats .
[ { "start": 40, "end": 53, "label": "Disease", "value": "renal failure" }, { "start": 109, "end": 119, "label": "Chemical", "value": "creatinine" }, { "start": 130, "end": 137, "label": "Chemical", "value": "lithium" } ]
en
NX caused an additive deterioration in GFR which , however , was ameliorated by HP .
[]
en
NX + HP caused a further rise in blood pressure in Li - pretreated rats .
[ { "start": 51, "end": 53, "label": "Chemical", "value": "Li" } ]
en
The results indicate that Li - induced nephropathy , even when the GFR is only modestly reduced , is associated with proteinuria and arterial systolic hypertension .
[ { "start": 26, "end": 28, "label": "Chemical", "value": "Li" }, { "start": 39, "end": 50, "label": "Disease", "value": "nephropathy" }, { "start": 117, "end": 128, "label": "Disease", "value": "proteinuria" }, { "start": 151, "end": 163, "label...
en
In this model of chronic renal failure
[ { "start": 17, "end": 38, "label": "Disease", "value": "chronic renal failure" } ]
en
Treatment of Crohn's disease with fusidic acid : an antibiotic with immunosuppressive properties similar to cyclosporin .
[ { "start": 13, "end": 28, "label": "Disease", "value": "Crohn's disease" }, { "start": 34, "end": 46, "label": "Chemical", "value": "fusidic acid" }, { "start": 108, "end": 119, "label": "Chemical", "value": "cyclosporin" } ]
en
Fusidic acid is an antibiotic with T - cell specific immunosuppressive effects similar to those of cyclosporin .
[ { "start": 99, "end": 110, "label": "Chemical", "value": "cyclosporin" } ]
en
Because of the need for the development of new treatments for Crohn's disease , a pilot study was undertaken to estimate the pharmacodynamics and tolerability of fusidic acid treatment in chronic active , therapy - resistant patients .
[ { "start": 62, "end": 77, "label": "Disease", "value": "Crohn's disease" }, { "start": 162, "end": 174, "label": "Chemical", "value": "fusidic acid" } ]
en
Eight Crohn's disease patients were included .
[ { "start": 6, "end": 21, "label": "Disease", "value": "Crohn's disease" } ]
en
Fusidic acid was administered orally in a dose of 500 mg t .
[ { "start": 0, "end": 12, "label": "Chemical", "value": "Fusidic acid" } ]
en
d .
[]
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s .
[]
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and the treatment was planned to last 8 weeks .
[]
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The disease activity was primarily measured by a modified individual grading score .
[]
en
Five of 8 patients ( 63 %) improved during fusidic acid treatment : 3 at two weeks and 2 after four weeks .
[ { "start": 43, "end": 55, "label": "Chemical", "value": "fusidic acid" } ]
en
There were no serious clinical side effects , but dose reduction was required in two patients because of nausea .
[ { "start": 105, "end": 111, "label": "Disease", "value": "nausea" } ]
en
Biochemically , an increase in alkaline phosphatases was noted in 5 of 8 cases ( 63 %), and the greatest increases were seen in those who had elevated levels prior to treatment .
[]
en
All reversed to pre - treatment levels after cessation of treatment .
[]
en
The results of this pilot study suggest that fusidic acid may be of benefit in selected chronic active Crohn's disease patients in whom conventional treatment is ineffective .
[ { "start": 45, "end": 57, "label": "Chemical", "value": "fusidic acid" }, { "start": 103, "end": 118, "label": "Disease", "value": "Crohn's disease" } ]
en
Because there seems to exist a scientific rationale for the use of fusidic acid at the cytokine level in inflammatory bowel disease
[ { "start": 67, "end": 79, "label": "Chemical", "value": "fusidic acid" }, { "start": 105, "end": 131, "label": "Disease", "value": "inflammatory bowel disease" } ]
en
Electrocardiographic evidence of myocardial injury in psychiatrically hospitalized cocaine abusers .
[ { "start": 33, "end": 50, "label": "Disease", "value": "myocardial injury" }, { "start": 83, "end": 90, "label": "Chemical", "value": "cocaine" } ]
en
The electrocardiograms ( ECG ) of 99 cocaine - abusing patients were compared with the ECGs of 50 schizophrenic controls .
[ { "start": 37, "end": 44, "label": "Chemical", "value": "cocaine" }, { "start": 98, "end": 111, "label": "Disease", "value": "schizophrenic" } ]
en
Eleven of the cocaine abusers and none of the controls had ECG evidence of significant myocardial injury defined as myocardial infarction , ischemia , and bundle branch block
[ { "start": 14, "end": 21, "label": "Chemical", "value": "cocaine" }, { "start": 87, "end": 104, "label": "Disease", "value": "myocardial injury" }, { "start": 116, "end": 137, "label": "Disease", "value": "myocardial infarction" }, { "start": 140, ...
en
Sulpiride - induced tardive dystonia .
[ { "start": 0, "end": 9, "label": "Chemical", "value": "Sulpiride" }, { "start": 20, "end": 36, "label": "Disease", "value": "tardive dystonia" } ]
en
Sulpiride is a selective D2 - receptor antagonist with antipsychotic and antidepressant properties .
[ { "start": 0, "end": 9, "label": "Chemical", "value": "Sulpiride" }, { "start": 73, "end": 87, "label": "Chemical", "value": "antidepressant" } ]
en
Although initially thought to be free of extrapyramidal side effects , sulpiride - induced tardive dyskinesia and parkinsonism have been reported occasionally .
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en
We studied a 37 - year - old man who developed persistent segmental dystonia within 2 months after starting sulpiride therapy .
[ { "start": 68, "end": 76, "label": "Disease", "value": "dystonia" }, { "start": 108, "end": 117, "label": "Chemical", "value": "sulpiride" } ]
en
We could not find any previous reports of sulpiride - induced tardive dystonia
[ { "start": 42, "end": 51, "label": "Chemical", "value": "sulpiride" }, { "start": 62, "end": 78, "label": "Disease", "value": "tardive dystonia" } ]
en
Ocular and auditory toxicity in hemodialyzed patients receiving desferrioxamine .
[ { "start": 0, "end": 28, "label": "Disease", "value": "Ocular and auditory toxicity" }, { "start": 64, "end": 79, "label": "Chemical", "value": "desferrioxamine" } ]
en
During an 18 - month period of study 41 hemodialyzed patients receiving desferrioxamine ( 10 - 40 mg / kg BW / 3 times weekly ) for the first time were monitored for detection of audiovisual toxicity .
[ { "start": 72, "end": 87, "label": "Chemical", "value": "desferrioxamine" }, { "start": 179, "end": 199, "label": "Disease", "value": "audiovisual toxicity" } ]
en
6 patients presented clinical symptoms of visual or auditory toxicity .
[ { "start": 42, "end": 69, "label": "Disease", "value": "visual or auditory toxicity" } ]
en
Moreover , detailed ophthalmologic and audiologic studies disclosed abnormalities in 7 more asymptomatic patients .
[]
en
Visual toxicity was of retinal origin and was characterized by a tritan - type dyschromatopsy , sometimes associated with a loss of visual acuity and pigmentary retinal deposits .
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en
Auditory toxicity was characterized by a mid - to high - frequency neurosensorial hearing loss and the lesion was of the cochlear type .
[ { "start": 0, "end": 17, "label": "Disease", "value": "Auditory toxicity" }, { "start": 67, "end": 94, "label": "Disease", "value": "neurosensorial hearing loss" } ]
en
Desferrioxamine withdrawal resulted in a complete recovery of visual function in 1 patient and partial recovery in 3 , and a complete reversal of hearing loss in 3 patients and partial recovery in 3 .
[ { "start": 0, "end": 15, "label": "Chemical", "value": "Desferrioxamine" }, { "start": 146, "end": 158, "label": "Disease", "value": "hearing loss" } ]
en
This toxicity appeared in patients receiving the higher doses of desferrioxamine or coincided with the normalization of ferritin or aluminium serum levels .
[ { "start": 5, "end": 13, "label": "Disease", "value": "toxicity" }, { "start": 65, "end": 80, "label": "Chemical", "value": "desferrioxamine" }, { "start": 132, "end": 141, "label": "Chemical", "value": "aluminium" } ]
en
The data indicate that audiovisual toxicity is not an infrequent complication in hemodialyzed patients receiving desferrioxamine
[ { "start": 23, "end": 43, "label": "Disease", "value": "audiovisual toxicity" }, { "start": 113, "end": 128, "label": "Chemical", "value": "desferrioxamine" } ]
en
Myasthenia gravis presenting as weakness after magnesium administration .
[ { "start": 0, "end": 17, "label": "Disease", "value": "Myasthenia gravis" }, { "start": 47, "end": 56, "label": "Chemical", "value": "magnesium" } ]
en
We studied a patient with no prior history of neuromuscular disease who became virtually quadriplegic after parenteral magnesium administration for preeclampsia .
[ { "start": 46, "end": 67, "label": "Disease", "value": "neuromuscular disease" }, { "start": 89, "end": 101, "label": "Disease", "value": "quadriplegic" }, { "start": 119, "end": 128, "label": "Chemical", "value": "magnesium" }, { "start": 148, "en...
en
The serum magnesium concentration was 3 .
[ { "start": 10, "end": 19, "label": "Chemical", "value": "magnesium" } ]
en
0 mEq / L , which is usually well tolerated .
[]
en
The magnesium was stopped and she recovered over a few days .
[ { "start": 4, "end": 13, "label": "Chemical", "value": "magnesium" } ]
en
While she was weak , 2 - Hz repetitive stimulation revealed a decrement without significant facilitation at rapid rates or after exercise , suggesting postsynaptic neuromuscular blockade .
[ { "start": 151, "end": 186, "label": "Disease", "value": "postsynaptic neuromuscular blockade" } ]
en
After her strength returned , repetitive stimulation was normal , but single fiber EMG revealed increased jitter and blocking .
[]
en
Her acetylcholine receptor antibody level was markedly elevated .
[ { "start": 4, "end": 17, "label": "Chemical", "value": "acetylcholine" } ]
en
Although paralysis after magnesium administration has been described in patients with known myasthenia gravis , it has not previously been reported to be the initial or only manifestation of the disease .
[ { "start": 9, "end": 18, "label": "Disease", "value": "paralysis" }, { "start": 25, "end": 34, "label": "Chemical", "value": "magnesium" }, { "start": 92, "end": 109, "label": "Disease", "value": "myasthenia gravis" } ]
en
Patients who are unusually sensitive to the neuromuscular effects of magnesium should be suspected of having an underlying disorder of neuromuscular transmission
[ { "start": 69, "end": 78, "label": "Chemical", "value": "magnesium" }, { "start": 123, "end": 161, "label": "Disease", "value": "disorder of neuromuscular transmission" } ]
en
Chloroacetaldehyde and its contribution to urotoxicity during treatment with cyclophosphamide or ifosfamide .
[ { "start": 0, "end": 18, "label": "Chemical", "value": "Chloroacetaldehyde" }, { "start": 77, "end": 93, "label": "Chemical", "value": "cyclophosphamide" }, { "start": 97, "end": 107, "label": "Chemical", "value": "ifosfamide" } ]
en
An experimental study / short communication .
[]
en
Based on clinical data , indicating that chloroacetaldehyde ( CAA ) is an important metabolite of oxazaphosphorine cytostatics , an experimental study was carried out in order to elucidate the role of CAA in the development of hemorrhagic cystitis .
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en
The data demonstrate that CAA after i .
[ { "start": 26, "end": 29, "label": "Chemical", "value": "CAA" } ]
en
v .
[]
en
administration does not contribute to bladder damage .
[ { "start": 38, "end": 52, "label": "Disease", "value": "bladder damage" } ]
en
When instilled directly into the bladder , CAA exerts urotoxic effects , it is , however , susceptible to detoxification with mesna
[ { "start": 43, "end": 46, "label": "Chemical", "value": "CAA" }, { "start": 126, "end": 131, "label": "Chemical", "value": "mesna" } ]
en
Source of pain and primitive dysfunction in migraine : an identical site ? Twenty common migraine patients received a one sided frontotemporal application of nitroglycerin ( 10 patients ) or placebo ointment ( 10 patients ) in a double blind study .
[ { "start": 10, "end": 14, "label": "Disease", "value": "pain" }, { "start": 44, "end": 52, "label": "Disease", "value": "migraine" }, { "start": 89, "end": 97, "label": "Disease", "value": "migraine" }, { "start": 158, "end": 171, "label": "Che...
en
Early onset migraine attacks were induced by nitroglycerin in seven out of 10 patients versus no patient in the placebo group .
[ { "start": 12, "end": 20, "label": "Disease", "value": "migraine" }, { "start": 45, "end": 58, "label": "Chemical", "value": "nitroglycerin" } ]
en
Subsequently 20 migraine patients , who developed an early onset attack with frontotemporal nitroglycerin , received the drug in a second induction test at other body areas .
[ { "start": 16, "end": 24, "label": "Disease", "value": "migraine" }, { "start": 92, "end": 105, "label": "Chemical", "value": "nitroglycerin" } ]
en
No early onset migraine was observed .
[ { "start": 15, "end": 23, "label": "Disease", "value": "migraine" } ]
en
Thus the migraine - inducing effect of nitroglycerin seems to depend on direct stimulation of the habitual site of pain , suggesting that the frontotemporal region is of crucial importance in the development of a migraine crisis .
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en
This is not consistent with a CNS origin of migraine
[ { "start": 44, "end": 52, "label": "Disease", "value": "migraine" } ]
en
Clotiazepam - induced acute hepatitis .
[ { "start": 0, "end": 11, "label": "Chemical", "value": "Clotiazepam" }, { "start": 28, "end": 37, "label": "Disease", "value": "hepatitis" } ]
en
We report the case of a patient who developed acute hepatitis with extensive hepatocellular necrosis , 7 months after the onset of administration of clotiazepam , a thienodiazepine derivative .
[ { "start": 52, "end": 61, "label": "Disease", "value": "hepatitis" }, { "start": 67, "end": 100, "label": "Disease", "value": "extensive hepatocellular necrosis" }, { "start": 149, "end": 160, "label": "Chemical", "value": "clotiazepam" }, { "start": 1...
en
Clotiazepam withdrawal was followed by prompt recovery .
[ { "start": 0, "end": 11, "label": "Chemical", "value": "Clotiazepam" } ]
en
The administration of several benzodiazepines , chemically related to clotiazepam , did not interfere with recovery and did not induce any relapse of hepatitis .
[ { "start": 30, "end": 45, "label": "Chemical", "value": "benzodiazepines" }, { "start": 70, "end": 81, "label": "Chemical", "value": "clotiazepam" }, { "start": 150, "end": 159, "label": "Disease", "value": "hepatitis" } ]
en
This observation shows that clotiazepam can induce acute hepatitis and suggests that there is no cross hepatotoxicity between clotiazepam and several benzodiazepines
[ { "start": 28, "end": 39, "label": "Chemical", "value": "clotiazepam" }, { "start": 57, "end": 66, "label": "Disease", "value": "hepatitis" }, { "start": 103, "end": 117, "label": "Disease", "value": "hepatotoxicity" }, { "start": 126, "end": 137, ...
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