@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP606805.RAH3xkeLAGjozR7u80xEmJq1bONZQylIphdL0gzyXMKMU130_head { this: np:hasAssertion dgn-np:NP606805.RAH3xkeLAGjozR7u80xEmJq1bONZQylIphdL0gzyXMKMU130_assertion; np:hasProvenance dgn-np:NP606805.RAH3xkeLAGjozR7u80xEmJq1bONZQylIphdL0gzyXMKMU130_provenance; np:hasPublicationInfo dgn-np:NP606805.RAH3xkeLAGjozR7u80xEmJq1bONZQylIphdL0gzyXMKMU130_publicationInfo; a np:Nanopublication . dgn-np:NP606805.RAH3xkeLAGjozR7u80xEmJq1bONZQylIphdL0gzyXMKMU130_assertion a np:Assertion . dgn-np:NP606805.RAH3xkeLAGjozR7u80xEmJq1bONZQylIphdL0gzyXMKMU130_provenance a np:Provenance . dgn-np:NP606805.RAH3xkeLAGjozR7u80xEmJq1bONZQylIphdL0gzyXMKMU130_publicationInfo a np:PublicationInfo . } dgn-np:NP606805.RAH3xkeLAGjozR7u80xEmJq1bONZQylIphdL0gzyXMKMU130_assertion { miriam-gene:5468 a ncit:C16612 . lld:C0011860 a ncit:C7057 . dgn-gda:DGN82953e93413a0fed8d415d7403a63861 sio:SIO_000628 miriam-gene:5468, lld:C0011860; a sio:SIO_001121 . } dgn-np:NP606805.RAH3xkeLAGjozR7u80xEmJq1bONZQylIphdL0gzyXMKMU130_provenance { dgn-np:NP606805.RAH3xkeLAGjozR7u80xEmJq1bONZQylIphdL0gzyXMKMU130_assertion dcterms:description "[We identify T2D-associated variants in an intergenic region of chromosome 11p12, contribute to the identification of T2D-associated variants near the genes IGF2BP2 and CDKAL1 and the region of CDKN2A and CDKN2B, and confirm that variants near TCF7L2, SLC30A8, HHEX, FTO, PPARG, and KCNJ11 are associated with T2D risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:17463248; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP606805.RAH3xkeLAGjozR7u80xEmJq1bONZQylIphdL0gzyXMKMU130_publicationInfo { this: dcterms:created "2016-05-13T12:46:20+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }