@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:NP172568.RAyz4XfaKlACEGYuld6e_SkIcxSig9_KUXgELBx1YTrdM130_head { this: np:hasAssertion dgn-np:NP172568.RAyz4XfaKlACEGYuld6e_SkIcxSig9_KUXgELBx1YTrdM130_assertion; np:hasProvenance dgn-np:NP172568.RAyz4XfaKlACEGYuld6e_SkIcxSig9_KUXgELBx1YTrdM130_provenance; np:hasPublicationInfo dgn-np:NP172568.RAyz4XfaKlACEGYuld6e_SkIcxSig9_KUXgELBx1YTrdM130_publicationInfo; a np:Nanopublication . dgn-np:NP172568.RAyz4XfaKlACEGYuld6e_SkIcxSig9_KUXgELBx1YTrdM130_assertion a np:Assertion . dgn-np:NP172568.RAyz4XfaKlACEGYuld6e_SkIcxSig9_KUXgELBx1YTrdM130_provenance a np:Provenance . dgn-np:NP172568.RAyz4XfaKlACEGYuld6e_SkIcxSig9_KUXgELBx1YTrdM130_publicationInfo a np:PublicationInfo . } dgn-np:NP172568.RAyz4XfaKlACEGYuld6e_SkIcxSig9_KUXgELBx1YTrdM130_assertion { miriam-gene:9370 a ncit:C16612 . lld:C0011860 a ncit:C7057 . dgn-gda:DGN78bee243a8720bd2780fce61984334bd sio:SIO_000628 miriam-gene:9370, lld:C0011860; a sio:SIO_001122 . } dgn-np:NP172568.RAyz4XfaKlACEGYuld6e_SkIcxSig9_KUXgELBx1YTrdM130_provenance { dgn-np:NP172568.RAyz4XfaKlACEGYuld6e_SkIcxSig9_KUXgELBx1YTrdM130_assertion dcterms:description "[The analyses showed that age (P < 0.0001), BMI (P < 0.0001), and six variants (IGF2BP2 rs4402960, P = 0.002; ADIPOQ+276 G>T, P = 0.004; UCP2Ala55Val, P = 0.01; CDKN2AI2B rs3731201, P = 0.02; rs495490, P = 0.02, and rsl 0811661, P = 0.03) were significantly associated with the risk of IFG/IGT/T2DM.]. 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:20384434; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP172568.RAyz4XfaKlACEGYuld6e_SkIcxSig9_KUXgELBx1YTrdM130_publicationInfo { this: dcterms:created "2016-05-13T12:43:05+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" . }