@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:NP1274884.RAHqp96Q6KNYhI4XgPT1qknas-CpLWcn6-1R17MHaRtHk130_head { this: np:hasAssertion dgn-np:NP1274884.RAHqp96Q6KNYhI4XgPT1qknas-CpLWcn6-1R17MHaRtHk130_assertion; np:hasProvenance dgn-np:NP1274884.RAHqp96Q6KNYhI4XgPT1qknas-CpLWcn6-1R17MHaRtHk130_provenance; np:hasPublicationInfo dgn-np:NP1274884.RAHqp96Q6KNYhI4XgPT1qknas-CpLWcn6-1R17MHaRtHk130_publicationInfo; a np:Nanopublication . dgn-np:NP1274884.RAHqp96Q6KNYhI4XgPT1qknas-CpLWcn6-1R17MHaRtHk130_assertion a np:Assertion . dgn-np:NP1274884.RAHqp96Q6KNYhI4XgPT1qknas-CpLWcn6-1R17MHaRtHk130_provenance a np:Provenance . dgn-np:NP1274884.RAHqp96Q6KNYhI4XgPT1qknas-CpLWcn6-1R17MHaRtHk130_publicationInfo a np:PublicationInfo . } dgn-np:NP1274884.RAHqp96Q6KNYhI4XgPT1qknas-CpLWcn6-1R17MHaRtHk130_assertion { miriam-gene:1135 a ncit:C16612 . lld:C0948750 a ncit:C7057 . dgn-gda:DGN86016268cf8ecde89df8c1dd8811f903 sio:SIO_000628 miriam-gene:1135, lld:C0948750; a sio:SIO_001121 . } dgn-np:NP1274884.RAHqp96Q6KNYhI4XgPT1qknas-CpLWcn6-1R17MHaRtHk130_provenance { dgn-np:NP1274884.RAHqp96Q6KNYhI4XgPT1qknas-CpLWcn6-1R17MHaRtHk130_assertion dcterms:description "[A genome-wide significant association with SGC in non-Hispanic white individuals was detected at coding SNPs in CHRNA2 (cholinergic receptor, nicotinic, alpha 2 [neuronal]) (OR, 8.55; 95% CI, 4.53-16.13 [P = 3.6 × 10(-11)]), OR4F15 (olfactory receptor, family 4, subfamily F, member 15) (OR, 5.26; 95% CI, 3.13-8.83 [P = 3.5 × 10(-10)]), ZNF343 (zinc finger protein 343) (OR, 3.28; 95% CI, 2.12-5.07 [P = 9.1 × 10(-8)]), and PARP4 (poly(ADP-ribose) polymerase family, member 4) (OR, 2.00; 95% CI, 1.54-2.59 [P = 1.7 × 10(-7)]).]. 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:25823930; 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:NP1274884.RAHqp96Q6KNYhI4XgPT1qknas-CpLWcn6-1R17MHaRtHk130_publicationInfo { this: dcterms:created "2016-05-13T12:51:24+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" . }