@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:NP1005015.RAnjMi_XVMMiDqlfjTsbHd4Plc6xWz0DSSQq4-6Mw9At8130_head { this: np:hasAssertion dgn-np:NP1005015.RAnjMi_XVMMiDqlfjTsbHd4Plc6xWz0DSSQq4-6Mw9At8130_assertion; np:hasProvenance dgn-np:NP1005015.RAnjMi_XVMMiDqlfjTsbHd4Plc6xWz0DSSQq4-6Mw9At8130_provenance; np:hasPublicationInfo dgn-np:NP1005015.RAnjMi_XVMMiDqlfjTsbHd4Plc6xWz0DSSQq4-6Mw9At8130_publicationInfo; a np:Nanopublication . dgn-np:NP1005015.RAnjMi_XVMMiDqlfjTsbHd4Plc6xWz0DSSQq4-6Mw9At8130_assertion a np:Assertion . dgn-np:NP1005015.RAnjMi_XVMMiDqlfjTsbHd4Plc6xWz0DSSQq4-6Mw9At8130_provenance a np:Provenance . dgn-np:NP1005015.RAnjMi_XVMMiDqlfjTsbHd4Plc6xWz0DSSQq4-6Mw9At8130_publicationInfo a np:PublicationInfo . } dgn-np:NP1005015.RAnjMi_XVMMiDqlfjTsbHd4Plc6xWz0DSSQq4-6Mw9At8130_assertion { miriam-gene:6934 a ncit:C16612 . lld:C0011860 a ncit:C7057 . dgn-gda:DGN4b7965e1a913769d53660d0d4e035064 sio:SIO_000628 miriam-gene:6934, lld:C0011860; a sio:SIO_001121 . } dgn-np:NP1005015.RAnjMi_XVMMiDqlfjTsbHd4Plc6xWz0DSSQq4-6Mw9At8130_provenance { dgn-np:NP1005015.RAnjMi_XVMMiDqlfjTsbHd4Plc6xWz0DSSQq4-6Mw9At8130_assertion dcterms:description "[Results from current association studies on T2DM susceptible genes in GDM have shown significant heterogeneity There may be primary evidence that polymorphisms of susceptible genes of T2DM such as transcription factor 7-like 2 (TCF7L2) gene, potassium channel voltage-gate KQT-like subfamily member 1 (KCNQ1) gene, and cyclin-dependent kinase 5 regulatory subunit-associated protein 1-like 1 (CDKAL1) gene, may increase risk of GDM.]. 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:22891507; 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:NP1005015.RAnjMi_XVMMiDqlfjTsbHd4Plc6xWz0DSSQq4-6Mw9At8130_publicationInfo { this: dcterms:created "2016-05-13T12:49:21+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" . }