@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:NP346378.RABI2oCxf_KKOd7AY_cWobicu-VoKJdbpI7Piz9VXPSs8130_head { this: np:hasAssertion dgn-np:NP346378.RABI2oCxf_KKOd7AY_cWobicu-VoKJdbpI7Piz9VXPSs8130_assertion; np:hasProvenance dgn-np:NP346378.RABI2oCxf_KKOd7AY_cWobicu-VoKJdbpI7Piz9VXPSs8130_provenance; np:hasPublicationInfo dgn-np:NP346378.RABI2oCxf_KKOd7AY_cWobicu-VoKJdbpI7Piz9VXPSs8130_publicationInfo; a np:Nanopublication . dgn-np:NP346378.RABI2oCxf_KKOd7AY_cWobicu-VoKJdbpI7Piz9VXPSs8130_assertion a np:Assertion . dgn-np:NP346378.RABI2oCxf_KKOd7AY_cWobicu-VoKJdbpI7Piz9VXPSs8130_provenance a np:Provenance . dgn-np:NP346378.RABI2oCxf_KKOd7AY_cWobicu-VoKJdbpI7Piz9VXPSs8130_publicationInfo a np:PublicationInfo . } dgn-np:NP346378.RABI2oCxf_KKOd7AY_cWobicu-VoKJdbpI7Piz9VXPSs8130_assertion { miriam-gene:1594 a ncit:C16612 . lld:C1847835 a ncit:C7057 . dgn-gda:DGN9f48ed4641a8ac888bfd95b9b4ca6ea8 sio:SIO_000628 miriam-gene:1594, lld:C1847835; a sio:SIO_001121 . } dgn-np:NP346378.RABI2oCxf_KKOd7AY_cWobicu-VoKJdbpI7Piz9VXPSs8130_provenance { dgn-np:NP346378.RABI2oCxf_KKOd7AY_cWobicu-VoKJdbpI7Piz9VXPSs8130_assertion dcterms:description "[Genetic variations within the vitamin D receptor (VDR) gene could lead to significant receptor dysfunction, and could further affect the formation of the biologically active 25(OH)D. Therefore, we hypothesized that VDR polymorphisms might be involved in vitiligo by affecting the formation of 25(OH)D.]. 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:22762534; 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:NP346378.RABI2oCxf_KKOd7AY_cWobicu-VoKJdbpI7Piz9VXPSs8130_publicationInfo { this: dcterms:created "2015-08-25T14:40:59+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" . }