@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:NP335813.RA6FWH-zmGrMqF4vMAjalPnR_IjDF9Enm2hI9WJ3GRUIQ130_head { this: np:hasAssertion dgn-np:NP335813.RA6FWH-zmGrMqF4vMAjalPnR_IjDF9Enm2hI9WJ3GRUIQ130_assertion; np:hasProvenance dgn-np:NP335813.RA6FWH-zmGrMqF4vMAjalPnR_IjDF9Enm2hI9WJ3GRUIQ130_provenance; np:hasPublicationInfo dgn-np:NP335813.RA6FWH-zmGrMqF4vMAjalPnR_IjDF9Enm2hI9WJ3GRUIQ130_publicationInfo; a np:Nanopublication . dgn-np:NP335813.RA6FWH-zmGrMqF4vMAjalPnR_IjDF9Enm2hI9WJ3GRUIQ130_assertion a np:Assertion . dgn-np:NP335813.RA6FWH-zmGrMqF4vMAjalPnR_IjDF9Enm2hI9WJ3GRUIQ130_provenance a np:Provenance . dgn-np:NP335813.RA6FWH-zmGrMqF4vMAjalPnR_IjDF9Enm2hI9WJ3GRUIQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP335813.RA6FWH-zmGrMqF4vMAjalPnR_IjDF9Enm2hI9WJ3GRUIQ130_assertion { miriam-gene:1493 a ncit:C16612 . lld:C1304470 a ncit:C7057 . dgn-gda:DGN1032600a6626f5d53d89ad30c51fee4b sio:SIO_000628 miriam-gene:1493, lld:C1304470; a sio:SIO_001122 . } dgn-np:NP335813.RA6FWH-zmGrMqF4vMAjalPnR_IjDF9Enm2hI9WJ3GRUIQ130_provenance { dgn-np:NP335813.RA6FWH-zmGrMqF4vMAjalPnR_IjDF9Enm2hI9WJ3GRUIQ130_assertion dcterms:description "[Examination of five SNPs in the CTLA4 gene (rs1863800, rs231775, rs3087243, rs11571302, rs11571297, rs10932037) in the same 126 families yielded no evidence of allelic or genotypic association with either generalized vitiligo or the expanded autoimmune phenotype.]. 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:18200060; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP335813.RA6FWH-zmGrMqF4vMAjalPnR_IjDF9Enm2hI9WJ3GRUIQ130_publicationInfo { this: dcterms:created "2015-08-25T14:40:53+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }