@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:NP301747.RArMAQLC_jy0dI5xoV0yQW7shZsJpFjTMJVJSNXUrmHjQ130_head { this: np:hasAssertion dgn-np:NP301747.RArMAQLC_jy0dI5xoV0yQW7shZsJpFjTMJVJSNXUrmHjQ130_assertion; np:hasProvenance dgn-np:NP301747.RArMAQLC_jy0dI5xoV0yQW7shZsJpFjTMJVJSNXUrmHjQ130_provenance; np:hasPublicationInfo dgn-np:NP301747.RArMAQLC_jy0dI5xoV0yQW7shZsJpFjTMJVJSNXUrmHjQ130_publicationInfo; a np:Nanopublication . dgn-np:NP301747.RArMAQLC_jy0dI5xoV0yQW7shZsJpFjTMJVJSNXUrmHjQ130_assertion a np:Assertion . dgn-np:NP301747.RArMAQLC_jy0dI5xoV0yQW7shZsJpFjTMJVJSNXUrmHjQ130_provenance a np:Provenance . dgn-np:NP301747.RArMAQLC_jy0dI5xoV0yQW7shZsJpFjTMJVJSNXUrmHjQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP301747.RArMAQLC_jy0dI5xoV0yQW7shZsJpFjTMJVJSNXUrmHjQ130_assertion { miriam-gene:1020 a ncit:C16612 . lld:C0011860 a ncit:C7057 . dgn-gda:DGN3c9f852fb1c05a3ed4d4840feff8f7fc sio:SIO_000628 miriam-gene:1020, lld:C0011860; a sio:SIO_001121 . } dgn-np:NP301747.RArMAQLC_jy0dI5xoV0yQW7shZsJpFjTMJVJSNXUrmHjQ130_provenance { dgn-np:NP301747.RArMAQLC_jy0dI5xoV0yQW7shZsJpFjTMJVJSNXUrmHjQ130_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-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP301747.RArMAQLC_jy0dI5xoV0yQW7shZsJpFjTMJVJSNXUrmHjQ130_publicationInfo { this: dcterms:created "2015-08-25T14:40:33+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }