--- language: - en bigbio_language: - English license: cc-by-nc-3.0 multilinguality: monolingual bigbio_license_shortname: CC_BY_NC_3p0 pretty_name: miRNA homepage: https://www.scai.fraunhofer.de/en/business-research-areas/bioinformatics/downloads/download-mirna-test-corpus.html bigbio_pubmed: True bigbio_public: True bigbio_tasks: - NAMED_ENTITY_RECOGNITION - NAMED_ENTITY_DISAMBIGUATION --- # Dataset Card for miRNA ## Dataset Description - **Homepage:** https://www.scai.fraunhofer.de/en/business-research-areas/bioinformatics/downloads/download-mirna-test-corpus.html - **Pubmed:** True - **Public:** True - **Tasks:** NER,NED The corpus consists of 301 Medline citations. The documents were screened for mentions of miRNA in the abstract text. Gene, disease and miRNA entities were manually annotated. The corpus comprises of two separate files, a train and a test set, coming from 201 and 100 documents respectively. ## Citation Information ``` @Article{Bagewadi2014, author={Bagewadi, Shweta and Bobi{'{c}}, Tamara and Hofmann-Apitius, Martin and Fluck, Juliane and Klinger, Roman}, title={Detecting miRNA Mentions and Relations in Biomedical Literature}, journal={F1000Research}, year={2014}, month={Aug}, day={28}, publisher={F1000Research}, volume={3}, pages={205-205}, keywords={MicroRNAs; corpus; prediction algorithms}, abstract={ INTRODUCTION: MicroRNAs (miRNAs) have demonstrated their potential as post-transcriptional gene expression regulators, participating in a wide spectrum of regulatory events such as apoptosis, differentiation, and stress response. Apart from the role of miRNAs in normal physiology, their dysregulation is implicated in a vast array of diseases. Dissection of miRNA-related associations are valuable for contemplating their mechanism in diseases, leading to the discovery of novel miRNAs for disease prognosis, diagnosis, and therapy. MOTIVATION: Apart from databases and prediction tools, miRNA-related information is largely available as unstructured text. Manual retrieval of these associations can be labor-intensive due to steadily growing number of publications. Additionally, most of the published miRNA entity recognition methods are keyword based, further subjected to manual inspection for retrieval of relations. Despite the fact that several databases host miRNA-associations derived from text, lower sensitivity and lack of published details for miRNA entity recognition and associated relations identification has motivated the need for developing comprehensive methods that are freely available for the scientific community. Additionally, the lack of a standard corpus for miRNA-relations has caused difficulty in evaluating the available systems. We propose methods to automatically extract mentions of miRNAs, species, genes/proteins, disease, and relations from scientific literature. Our generated corpora, along with dictionaries, and miRNA regular expression are freely available for academic purposes. To our knowledge, these resources are the most comprehensive developed so far. RESULTS: The identification of specific miRNA mentions reaches a recall of 0.94 and precision of 0.93. Extraction of miRNA-disease and miRNA-gene relations lead to an F1 score of up to 0.76. A comparison of the information extracted by our approach to the databases miR2Disease and miRSel for the extraction of Alzheimer's disease related relations shows the capability of our proposed methods in identifying correct relations with improved sensitivity. The published resources and described methods can help the researchers for maximal retrieval of miRNA-relations and generation of miRNA-regulatory networks. AVAILABILITY: The training and test corpora, annotation guidelines, developed dictionaries, and supplementary files are available at http://www.scai.fraunhofer.de/mirna-corpora.html. }, note={26535109[pmid]}, note={PMC4602280[pmcid]}, issn={2046-1402}, url={https://pubmed.ncbi.nlm.nih.gov/26535109}, language={eng} } ```