@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:NP880094.RAolXKE1gFI0Nrk_DzFAb7s7OFyJ9Sp5F8sBjD9aUlSoE130_head { this: np:hasAssertion dgn-np:NP880094.RAolXKE1gFI0Nrk_DzFAb7s7OFyJ9Sp5F8sBjD9aUlSoE130_assertion; np:hasProvenance dgn-np:NP880094.RAolXKE1gFI0Nrk_DzFAb7s7OFyJ9Sp5F8sBjD9aUlSoE130_provenance; np:hasPublicationInfo dgn-np:NP880094.RAolXKE1gFI0Nrk_DzFAb7s7OFyJ9Sp5F8sBjD9aUlSoE130_publicationInfo; a np:Nanopublication . dgn-np:NP880094.RAolXKE1gFI0Nrk_DzFAb7s7OFyJ9Sp5F8sBjD9aUlSoE130_assertion a np:Assertion . dgn-np:NP880094.RAolXKE1gFI0Nrk_DzFAb7s7OFyJ9Sp5F8sBjD9aUlSoE130_provenance a np:Provenance . dgn-np:NP880094.RAolXKE1gFI0Nrk_DzFAb7s7OFyJ9Sp5F8sBjD9aUlSoE130_publicationInfo a np:PublicationInfo . } dgn-np:NP880094.RAolXKE1gFI0Nrk_DzFAb7s7OFyJ9Sp5F8sBjD9aUlSoE130_assertion { miriam-gene:2571 a ncit:C16612 . lld:C0011860 a ncit:C7057 . dgn-gda:DGN1f2e9b49cd330f5e41113447b6714bb7 sio:SIO_000628 miriam-gene:2571, lld:C0011860; a sio:SIO_001122 . } dgn-np:NP880094.RAolXKE1gFI0Nrk_DzFAb7s7OFyJ9Sp5F8sBjD9aUlSoE130_provenance { dgn-np:NP880094.RAolXKE1gFI0Nrk_DzFAb7s7OFyJ9Sp5F8sBjD9aUlSoE130_assertion dcterms:description "[In 509 GAD-negative patients with newly diagnosed type 2 diabetes, we 1) genotyped six single nucleotide polymorphisms in GCKR genomic region: rs6717980, rs1049817, rs6547626, rs780094, rs2384628, and rs8731; 2) assessed clinical phenotypes, insulin sensitivity by the euglycemic insulin clamp, and β-cell function by state-of-the-art modeling of glucose/C-peptide curves during an oral glucose tolerance test; and 3) estimated glomerular filtration rate (eGFR) by the Modification of Diet in Renal Disease formula.]. 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:21411509; 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:NP880094.RAolXKE1gFI0Nrk_DzFAb7s7OFyJ9Sp5F8sBjD9aUlSoE130_publicationInfo { this: dcterms:created "2016-05-13T12:48:23+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" . }