@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:NP1288259.RAWhgt8s5xMrGK8C8AJlvQImtV4or4Sdf_JRxAEvZ57fQ130_head { this: np:hasAssertion dgn-np:NP1288259.RAWhgt8s5xMrGK8C8AJlvQImtV4or4Sdf_JRxAEvZ57fQ130_assertion; np:hasProvenance dgn-np:NP1288259.RAWhgt8s5xMrGK8C8AJlvQImtV4or4Sdf_JRxAEvZ57fQ130_provenance; np:hasPublicationInfo dgn-np:NP1288259.RAWhgt8s5xMrGK8C8AJlvQImtV4or4Sdf_JRxAEvZ57fQ130_publicationInfo; a np:Nanopublication . dgn-np:NP1288259.RAWhgt8s5xMrGK8C8AJlvQImtV4or4Sdf_JRxAEvZ57fQ130_assertion a np:Assertion . dgn-np:NP1288259.RAWhgt8s5xMrGK8C8AJlvQImtV4or4Sdf_JRxAEvZ57fQ130_provenance a np:Provenance . dgn-np:NP1288259.RAWhgt8s5xMrGK8C8AJlvQImtV4or4Sdf_JRxAEvZ57fQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP1288259.RAWhgt8s5xMrGK8C8AJlvQImtV4or4Sdf_JRxAEvZ57fQ130_assertion { miriam-gene:1230 a ncit:C16612 . lld:C0004943 a ncit:C7057 . dgn-gda:DGN6e2b05c471ac3d006e7da02d8a0d6a67 sio:SIO_000628 miriam-gene:1230, lld:C0004943; a sio:SIO_001122 . } dgn-np:NP1288259.RAWhgt8s5xMrGK8C8AJlvQImtV4or4Sdf_JRxAEvZ57fQ130_provenance { dgn-np:NP1288259.RAWhgt8s5xMrGK8C8AJlvQImtV4or4Sdf_JRxAEvZ57fQ130_assertion dcterms:description "[Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).]. 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:26097239; 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:NP1288259.RAWhgt8s5xMrGK8C8AJlvQImtV4or4Sdf_JRxAEvZ57fQ130_publicationInfo { this: dcterms:created "2016-05-13T12:51:30+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" . }