@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:NP220360.RAbazMA7tBHPxZKGcrf6r88_iBmvfxo1RGiHJrN0zxpbg130_head { this: np:hasAssertion dgn-np:NP220360.RAbazMA7tBHPxZKGcrf6r88_iBmvfxo1RGiHJrN0zxpbg130_assertion; np:hasProvenance dgn-np:NP220360.RAbazMA7tBHPxZKGcrf6r88_iBmvfxo1RGiHJrN0zxpbg130_provenance; np:hasPublicationInfo dgn-np:NP220360.RAbazMA7tBHPxZKGcrf6r88_iBmvfxo1RGiHJrN0zxpbg130_publicationInfo; a np:Nanopublication . dgn-np:NP220360.RAbazMA7tBHPxZKGcrf6r88_iBmvfxo1RGiHJrN0zxpbg130_assertion a np:Assertion . dgn-np:NP220360.RAbazMA7tBHPxZKGcrf6r88_iBmvfxo1RGiHJrN0zxpbg130_provenance a np:Provenance . dgn-np:NP220360.RAbazMA7tBHPxZKGcrf6r88_iBmvfxo1RGiHJrN0zxpbg130_publicationInfo a np:PublicationInfo . } dgn-np:NP220360.RAbazMA7tBHPxZKGcrf6r88_iBmvfxo1RGiHJrN0zxpbg130_assertion { miriam-gene:3784 a ncit:C16612 . lld:C0011860 a ncit:C7057 . dgn-gda:DGN088aa07ebafdef0df06a2c23bd3cb085 sio:SIO_000628 miriam-gene:3784, lld:C0011860; a sio:SIO_001121 . } dgn-np:NP220360.RAbazMA7tBHPxZKGcrf6r88_iBmvfxo1RGiHJrN0zxpbg130_provenance { dgn-np:NP220360.RAbazMA7tBHPxZKGcrf6r88_iBmvfxo1RGiHJrN0zxpbg130_assertion dcterms:description "[In Chinese Han, we replicated the associations between 7 genetic loci and T2D, with risk allele-specific odds ratios (ORs) as follows: 1.27 (95% CI, 1.11-1.45; p = 0.0008) for CDKAL1-rs10946398, 1.26 (95% CI, 1.08-1.47; p = 0.003) for IGF2BP2-rs4402960, 1.19 (95% CI, 1.04-1.37; p = 0.009) for SLC30A8-rs13266634, 1.22 (95% CI, 1.06-1.41; p = 0.005) for CDKN2A/B-rs10811661, 1.20 (95% CI, 1.01-1.42; p = 0.03) for HHEX-rs5015480, 1.37 (95% CI, 1.19-1.69; p = 1.0 x 10(-4)) for KCNQ1-rs2237892, and 1.24 (95% CI, 1.01-1.52; p = 0.046) for FTO-rs8050136 after adjustment for age, gender, and body mass index.]. 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:20509872; 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:NP220360.RAbazMA7tBHPxZKGcrf6r88_iBmvfxo1RGiHJrN0zxpbg130_publicationInfo { this: dcterms:created "2014-10-02T12:34:02+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" . }