DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes.

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dc.contributor.author	Piñero González, Janet, 1977-
dc.contributor.author	Queralt Rosinach, Núria
dc.contributor.author	Bravo Serrano, Àlex, 1984-
dc.contributor.author	Déu Pons, Jordi
dc.contributor.author	Bauer-Mehren, Anna
dc.contributor.author	Baron, Martin
dc.contributor.author	Sanz, Ferran
dc.contributor.author	Furlong, Laura I., 1971-
dc.date	2015
dc.identifier.citation	Piñero J, Queralt-Rosinach N, Bravo À, Deu-Pons J, Bauer-Mehren A, Baron M. et al. DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes. Database (Oxford). 2015 Apr 15;2015:bav028. doi: 10.1093/database/bav028.
dc.identifier.citation	1758-0463
dc.identifier.citation	http://dx.doi.org/10.1093/database/bav028
dc.identifier.uri	http://hdl.handle.net/10230/23781
dc.format	application/pdf
dc.language.iso	eng
dc.publisher	Oxford University Press
dc.relation	info:eu-repo/grantAgreement/EC/FP7/115002
dc.relation	info:eu-repo/grantAgreement/EC/FP7/115191
dc.rights	c) Piñero J.et al. 2015. Published by Oxford University Press./nThis is an Open Access article distributed under the terms of the Creative Commons Attribution License https://creativecommons.org/licenses/by/4.0/, which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.rights	https://creativecommons.org/licenses/by/4.0/
dc.rights	info:eu-repo/semantics/openAccess
dc.subject	Genètica humana
dc.subject	Bases de dades
dc.title	DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes.
dc.type	info:eu-repo/semantics/article
dc.type	info:eu-repo/semantics/publishedVersion
dc.description.abstract	DisGeNET is a comprehensive discovery platform designed to address a variety of questions concerning the genetic underpinning of human diseases. DisGeNET contains over 380,000 associations between >16,000 genes and 13,000 diseases, which makes it one of the largest repositories currently available of its kind. DisGeNET integrates expert-curated databases with text-mined data, covers information on Mendelian and complex diseases, and includes data from animal disease models. It features a score based on the supporting evidence to prioritize gene-disease associations. It is an open access resource available through a web interface, a Cytoscape plugin and as a Semantic Web resource. The web interface supports user-friendly data exploration and navigation. DisGeNET data can also be analysed via the DisGeNET Cytoscape plugin, and enriched with the annotations of other plugins of this popular network analysis software suite. Finally, the information contained in DisGeNET can be expanded and complemented using Semantic Web technologies and linked to a variety of resources already present in the Linked Data cloud. Hence, DisGeNET offers one of the most comprehensive collections of human gene-disease associations and a valuable set of tools for investigating the molecular mechanisms underlying diseases of genetic origin, designed to fulfill the needs of different user profiles, including bioinformaticians, biologists and health-care practitioners. Database URL: http://www.disgenet.org/
dc.description.abstract	This work was supported by Instituto de Salud Carlos III-Fondo Europeo de Desarrollo Regional (CP10/00524 and PI13/00082), the/nInnovative Medicines Initiative Joint Undertaking (115002 (eTOX), 115191 [Open PHACTS]), resources of which are composed of financial/ncontribution from the European Union’s Seventh Framework Programme [FP7/2007-2013] and EFPIA companies’ in kind contribution./nThe Research Programme on Biomedical Informatics (GRIB) is a node of the Spanish National Institute of Bioinformatics (INB). Funding for open access charge: Instituto de Salud Carlos III-Fondo Europeo de Desarrollo Regional (PI13/00082).

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