@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:NP1321508.RADWFMd0CMS0Ya9eNJvoKjNiMgDNiZjvmiO7LNu7Cu-_M130_head { this: np:hasAssertion dgn-np:NP1321508.RADWFMd0CMS0Ya9eNJvoKjNiMgDNiZjvmiO7LNu7Cu-_M130_assertion; np:hasProvenance dgn-np:NP1321508.RADWFMd0CMS0Ya9eNJvoKjNiMgDNiZjvmiO7LNu7Cu-_M130_provenance; np:hasPublicationInfo dgn-np:NP1321508.RADWFMd0CMS0Ya9eNJvoKjNiMgDNiZjvmiO7LNu7Cu-_M130_publicationInfo; a np:Nanopublication . dgn-np:NP1321508.RADWFMd0CMS0Ya9eNJvoKjNiMgDNiZjvmiO7LNu7Cu-_M130_assertion a np:Assertion . dgn-np:NP1321508.RADWFMd0CMS0Ya9eNJvoKjNiMgDNiZjvmiO7LNu7Cu-_M130_provenance a np:Provenance . dgn-np:NP1321508.RADWFMd0CMS0Ya9eNJvoKjNiMgDNiZjvmiO7LNu7Cu-_M130_publicationInfo a np:PublicationInfo . } dgn-np:NP1321508.RADWFMd0CMS0Ya9eNJvoKjNiMgDNiZjvmiO7LNu7Cu-_M130_assertion { miriam-gene:3630 a ncit:C16612 . lld:C0011860 a ncit:C7057 . dgn-gda:DGN85c0c56e1077c52bdc2b10df5ac2d6d9 sio:SIO_000628 miriam-gene:3630, lld:C0011860; a sio:SIO_001121 . } dgn-np:NP1321508.RADWFMd0CMS0Ya9eNJvoKjNiMgDNiZjvmiO7LNu7Cu-_M130_provenance { dgn-np:NP1321508.RADWFMd0CMS0Ya9eNJvoKjNiMgDNiZjvmiO7LNu7Cu-_M130_assertion dcterms:description "[We therefore conclude that since the earliest defects identified in a group genetically at high risk to develop NIDDM are those related to insulin secretion, defects in insulin secretion rather than insulin sensitivity are likely the major genetic factor predisposing to development of NIDDM.]. 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:7776502; 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:NP1321508.RADWFMd0CMS0Ya9eNJvoKjNiMgDNiZjvmiO7LNu7Cu-_M130_publicationInfo { this: dcterms:created "2016-05-13T12:51:45+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" . }