pubmed-article:20214801 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20214801 | lifeskim:mentions | umls-concept:C0026336 | lld:lifeskim |
pubmed-article:20214801 | lifeskim:mentions | umls-concept:C0017431 | lld:lifeskim |
pubmed-article:20214801 | lifeskim:mentions | umls-concept:C0031437 | lld:lifeskim |
pubmed-article:20214801 | lifeskim:mentions | umls-concept:C1511726 | lld:lifeskim |
pubmed-article:20214801 | lifeskim:mentions | umls-concept:C0037585 | lld:lifeskim |
pubmed-article:20214801 | lifeskim:mentions | umls-concept:C0681814 | lld:lifeskim |
pubmed-article:20214801 | lifeskim:mentions | umls-concept:C1710360 | lld:lifeskim |
pubmed-article:20214801 | lifeskim:mentions | umls-concept:C0205375 | lld:lifeskim |
pubmed-article:20214801 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:20214801 | pubmed:dateCreated | 2010-5-6 | lld:pubmed |
pubmed-article:20214801 | pubmed:abstractText | We present an extensible software model for the genotype and phenotype community, XGAP. Readers can download a standard XGAP (http://www.xgap.org) or auto-generate a custom version using MOLGENIS with programming interfaces to R-software and web-services or user interfaces for biologists. XGAP has simple load formats for any type of genotype, epigenotype, transcript, protein, metabolite or other phenotype data. Current functionality includes tools ranging from eQTL analysis in mouse to genome-wide association studies in humans. | lld:pubmed |
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pubmed-article:20214801 | pubmed:language | eng | lld:pubmed |
pubmed-article:20214801 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20214801 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:20214801 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20214801 | pubmed:issn | 1465-6914 | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:JansenRitsert... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:SchughartKlau... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:HancockJohn... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:GobleCaroleC | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:SchofieldPaul... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:SmedleyDamian... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:SwertzMorris... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:AlbertsRudiR | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:JonesAndrew... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:WolstencroftK... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:ParkinsonHele... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:DijkstraMarti... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:VeraGonzaloG | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:ScheltemaRich... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:TessonBruno... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:VeldeK... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:ArendsDannyD | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:de... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:Coordination... | lld:pubmed |
pubmed-article:20214801 | pubmed:author | pubmed-author:Genotype-To-P... | lld:pubmed |
pubmed-article:20214801 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20214801 | pubmed:volume | 11 | lld:pubmed |
pubmed-article:20214801 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20214801 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20214801 | pubmed:pagination | R27 | lld:pubmed |
pubmed-article:20214801 | pubmed:dateRevised | 2010-9-28 | lld:pubmed |
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