@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:NP939409.RAlXLmfkg9DpGdl73r9ELMp9LMeeGLGIHZuedSGwPb-Gw130_head { this: np:hasAssertion dgn-np:NP939409.RAlXLmfkg9DpGdl73r9ELMp9LMeeGLGIHZuedSGwPb-Gw130_assertion; np:hasProvenance dgn-np:NP939409.RAlXLmfkg9DpGdl73r9ELMp9LMeeGLGIHZuedSGwPb-Gw130_provenance; np:hasPublicationInfo dgn-np:NP939409.RAlXLmfkg9DpGdl73r9ELMp9LMeeGLGIHZuedSGwPb-Gw130_publicationInfo; a np:Nanopublication . dgn-np:NP939409.RAlXLmfkg9DpGdl73r9ELMp9LMeeGLGIHZuedSGwPb-Gw130_assertion a np:Assertion . dgn-np:NP939409.RAlXLmfkg9DpGdl73r9ELMp9LMeeGLGIHZuedSGwPb-Gw130_provenance a np:Provenance . dgn-np:NP939409.RAlXLmfkg9DpGdl73r9ELMp9LMeeGLGIHZuedSGwPb-Gw130_publicationInfo a np:PublicationInfo . } dgn-np:NP939409.RAlXLmfkg9DpGdl73r9ELMp9LMeeGLGIHZuedSGwPb-Gw130_assertion { miriam-gene:3709 a ncit:C16612 . lld:C0007134 a ncit:C7057 . dgn-gda:DGN39de34c801d4852b5df904f5024d2489 sio:SIO_000628 miriam-gene:3709, lld:C0007134; a sio:SIO_001121 . } dgn-np:NP939409.RAlXLmfkg9DpGdl73r9ELMp9LMeeGLGIHZuedSGwPb-Gw130_provenance { dgn-np:NP939409.RAlXLmfkg9DpGdl73r9ELMp9LMeeGLGIHZuedSGwPb-Gw130_assertion dcterms:description "[We identified two common variants in linkage disequilibrium, rs718314 and rs1049380 (r(2) = 0.64, D ' = 0.84), in the inositol 1,4,5-triphosphate receptor, type 2 (ITPR2) gene on 12p11.23 as novel susceptibility loci for RCC (P = 8.89 × 10(-10) and P = 6.07 × 10(-9), respectively, in meta-analysis) with an allelic odds ratio of 1.19 [95% confidence interval (CI): 1.13-1.26] for rs718314 and 1.18 (95% CI: 1.12-1.25) for rs1049380.]. 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:22010048; 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:NP939409.RAlXLmfkg9DpGdl73r9ELMp9LMeeGLGIHZuedSGwPb-Gw130_publicationInfo { this: dcterms:created "2014-10-02T12:41:35+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" . }