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The Human Phenotype Ontology in 2017

dc.contributor.authorKoehler, Sen_US
dc.contributor.authorVasilevsky, NAen_US
dc.contributor.authorEngelstad, Men_US
dc.contributor.authorFoster, Een_US
dc.contributor.authorMcMurry, Jen_US
dc.contributor.authorAyme, Sen_US
dc.contributor.authorBaynam, Gen_US
dc.contributor.authorBello, SMen_US
dc.contributor.authorBoerkoel, CFen_US
dc.contributor.authorBoycott, KMen_US
dc.contributor.authorBrudno, Men_US
dc.contributor.authorBuske, OJen_US
dc.contributor.authorChinnery, PFen_US
dc.contributor.authorCipriani, Ven_US
dc.contributor.authorConnell, LEen_US
dc.contributor.authorDawkins, HJSen_US
dc.contributor.authorDeMare, LEen_US
dc.contributor.authorDevereau, ADen_US
dc.contributor.authorde Vries, BBAen_US
dc.contributor.authorFirth, HVen_US
dc.contributor.authorFreson, Ken_US
dc.contributor.authorGreene, Den_US
dc.contributor.authorHamosh, Aen_US
dc.contributor.authorHelbig, Ien_US
dc.contributor.authorHum, Cen_US
dc.contributor.authorJahn, JAen_US
dc.contributor.authorJames, Ren_US
dc.contributor.authorKrause, Ren_US
dc.contributor.authorLaulederkind, SJFen_US
dc.contributor.authorLochmuller, Hen_US
dc.contributor.authorLyon, GJen_US
dc.contributor.authorOgishima, Sen_US
dc.contributor.authorOlry, Aen_US
dc.contributor.authorOuwehand, WHen_US
dc.contributor.authorPontikos, Nen_US
dc.contributor.authorRath, Aen_US
dc.contributor.authorSchaefer, Fen_US
dc.contributor.authorScott, RHen_US
dc.contributor.authorSegal, Men_US
dc.contributor.authorSergouniotis, PIen_US
dc.contributor.authorSever, Ren_US
dc.contributor.authorSmith, CLen_US
dc.contributor.authorStraub, Ven_US
dc.contributor.authorThompson, Ren_US
dc.contributor.authorTurner, Cen_US
dc.contributor.authorTurro, Een_US
dc.contributor.authorVeltman, MWMen_US
dc.contributor.authorVulliamy, Ten_US
dc.contributor.authorYu, Jen_US
dc.contributor.authorvon Ziegenweidt, Jen_US
dc.contributor.authorZankl, Aen_US
dc.contributor.authorZuchner, Sen_US
dc.contributor.authorZemojtel, Ten_US
dc.contributor.authorJacobsen, JOBen_US
dc.contributor.authorGroza, Ten_US
dc.contributor.authorSmedley, Den_US
dc.contributor.authorMungall, CJen_US
dc.contributor.authorHaendel, Men_US
dc.contributor.authorRobinson, PNen_US
dc.date.accessioned2016-12-13T11:52:50Z
dc.date.available2016-10-28en_US
dc.date.issued2017-01-04en_US
dc.date.submitted2016-12-12T13:13:27.858Z
dc.identifier.issn0305-1048en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/18234
dc.description.sponsorshipNational Institutes of Health (NIH) Monarch Initiative [NIH OD #5R24OD011883]; E-RARE 2015 program, Hipbi-RD (harmonizing phenomics information for a better interoperability in the RD field); Director, Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy under [DE-AC02-05CH11231]; Bundesministerium f ¨ur Bildung und Forschung (BMBF) [0313911]; Raine Clinician Research Fellowship (to G.B.); Stanley Institute for Cognitive Genomics at Cold Spring Harbor Laboratory (CSHL to G.J.L.); European Union Seventh Framework Programme [FP7/2007-2013] supported RD-Connect [305444], EURenOmics [2012-305608] and NeurOmics [2012-305121]; Fight for Sight and Retinitis Pigmentosa Fighting Blindness (to N.P.); National Institute for Health Research Biomedical Research Centre at Moorfields Eye Hospital National Health Service Foundation Trust and UCL Institute of Ophthalmology (UK) (to V.C.); University of Kiel, by a grant from the German Research Foundation [HE5415/3-1 to I.H.] within the EuroEPINOMICS framework of the European Science Foundation and grants of the German Research Foundation [DFG, HE5415/5-1, HE5415/6-1], German Ministry for Education and Research [01DH12033, MAR 10/012] and by the German chapter of the International League against Epilepsy (DGfE); International League Against Epilepsy (ILAE to I.H.) within the Epilepsiome initiative of the ILAE Genetics Commission (www.channelopathist. net); National Library of Medicine [R44 LM011585-02 to M.S.]. BBAdV is funded by the Dutch Organisation for Health Research and Development (ZON-MW grants 912-12-109). Funding for open access charge: NIH [R24- OD011883]en_US
dc.format.extentD865 - D876en_US
dc.relation.ispartofNUCLEIC ACIDS RESEARCHen_US
dc.rightsCreative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/)
dc.rightsThis article has been accepted for publication in [Journal Title] Published by Oxford University Press.
dc.titleThe Human Phenotype Ontology in 2017en_US
dc.typeArticle
dc.rights.holder(c) The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research.
dc.identifier.doi10.1093/nar/gkw1039en_US
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000396575500121&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issueD1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume45en_US


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