@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:NP663193.RAxQSHVatQOegNqrg-HC7LBdle6Q0uyWgwc-TRbeVhFlc130_head { this: np:hasAssertion dgn-np:NP663193.RAxQSHVatQOegNqrg-HC7LBdle6Q0uyWgwc-TRbeVhFlc130_assertion; np:hasProvenance dgn-np:NP663193.RAxQSHVatQOegNqrg-HC7LBdle6Q0uyWgwc-TRbeVhFlc130_provenance; np:hasPublicationInfo dgn-np:NP663193.RAxQSHVatQOegNqrg-HC7LBdle6Q0uyWgwc-TRbeVhFlc130_publicationInfo; a np:Nanopublication . dgn-np:NP663193.RAxQSHVatQOegNqrg-HC7LBdle6Q0uyWgwc-TRbeVhFlc130_assertion a np:Assertion . dgn-np:NP663193.RAxQSHVatQOegNqrg-HC7LBdle6Q0uyWgwc-TRbeVhFlc130_provenance a np:Provenance . dgn-np:NP663193.RAxQSHVatQOegNqrg-HC7LBdle6Q0uyWgwc-TRbeVhFlc130_publicationInfo a np:PublicationInfo . } dgn-np:NP663193.RAxQSHVatQOegNqrg-HC7LBdle6Q0uyWgwc-TRbeVhFlc130_assertion { miriam-gene:391107 a ncit:C16612 . lld:C0011860 a ncit:C7057 . dgn-gda:DGN93ef00c78fc763b4619c7c8a158c5a91 sio:SIO_000628 miriam-gene:391107, lld:C0011860; a sio:SIO_001121 . } dgn-np:NP663193.RAxQSHVatQOegNqrg-HC7LBdle6Q0uyWgwc-TRbeVhFlc130_provenance { dgn-np:NP663193.RAxQSHVatQOegNqrg-HC7LBdle6Q0uyWgwc-TRbeVhFlc130_assertion dcterms:description "[The rs679931 TT genotype was associated with (1) an increased risk of type 2 diabetes in the Botnia case-control sample [odds ratio (OR) 1.4, 95% CI 1.0-2.0, p = 0.06] and in the replication sample (OR 1.2, 95% CI 1.0-1.5, p = 0.01 one-tailed), with a combined OR of 1.3 (95% CI 1.1-1.5, p = 0.004 two-tailed); (2) reduced insulin secretion [insulinogenic index at 30 min p = 0.02, disposition index (D (I)) p = 0.03] in control participants during an OGTT; (3) reduced second-phase insulin secretion at 30 min (p = 0.04) and 60 min (p = 0.02) during an IVGTT; and (4) reduced D (I) over time in the Botnia prospective cohort (p = 0.05).]. 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:17934712; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP663193.RAxQSHVatQOegNqrg-HC7LBdle6Q0uyWgwc-TRbeVhFlc130_publicationInfo { this: dcterms:created "2014-10-02T12:38:40+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }