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Proper Citation: DisGeNET (RRID:SCR_006178)
Description: Database and discovery platform containing publicly available collections of genes and variants associated to human diseases. Integrates data from curated repositories, GWAS catalogues, animal models and scientific literature.
Abbreviations: DisGeNET
Synonyms: database of gene disease associations
Resource Type: data or information resource, database
Defining Citation: PMID:27924018, PMID:25877637, PMID:21695124, PMID:20861032
Keywords: gene, disease, gene-disease association, gene-disease ontology, gene-disease text mining, text mining, genotype-phenotype, rdf, genotype, phenotype, gene-disease, variant-disease, FASEB list
Funding: EFPIA ; Elixir-Excelerate ; European Union Horizon 2020 ; European Union Seventh Framework Programme ; Innovative Medicines Initiative Joint Undertaking ; Instituto de Salud Carlos III-Fondo Europeo de Desarrollo Regional
Availability: Restricted
Resource Name: DisGeNET
Resource ID: SCR_006178
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
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