@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:NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_head { this: np:hasAssertion dgn-np:NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_assertion; np:hasProvenance dgn-np:NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance; np:hasPublicationInfo dgn-np:NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_publicationInfo; a np:Nanopublication . dgn-np:NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_assertion a np:Assertion . dgn-np:NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance a np:Provenance . dgn-np:NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_publicationInfo a np:PublicationInfo . } dgn-np:NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_assertion { miriam-gene:3815 a ncit:C16612 . lld:C0238198 a ncit:C7057 . dgn-gda:DGN18063fc3420e1d08d1970d8f0304a623 sio:SIO_000628 miriam-gene:3815, lld:C0238198; a sio:SIO_001122 . } dgn-np:NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance { dgn-np:NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_assertion dcterms:description "[Although none of the association p-values were statistically significant after adjustment for multiple comparisons, SNPs in CYP1B1 were strongly associated with KIT exon 11 codon 557-8 deletions (OR = 1.9, 95% CI: 1.3-2.9 for rs2855658 and OR = 1.8, 95% CI: 1.2-2.7 for rs1056836) and wild type GISTs (OR = 2.7, 95% CI: 1.5-4.8 for rs1800440 and OR = 0.5, 95% CI: 0.3-0.9 for rs1056836).]. 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:23637977; 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:NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_publicationInfo { this: dcterms:created "2016-05-13T12:49:53+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" . }