@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:NP1190648.RArfS1-vMbF6MCr0cX4vIzJE5qyCdmSNWlM3pkZhiCcwk130_head { this: np:hasAssertion dgn-np:NP1190648.RArfS1-vMbF6MCr0cX4vIzJE5qyCdmSNWlM3pkZhiCcwk130_assertion; np:hasProvenance dgn-np:NP1190648.RArfS1-vMbF6MCr0cX4vIzJE5qyCdmSNWlM3pkZhiCcwk130_provenance; np:hasPublicationInfo dgn-np:NP1190648.RArfS1-vMbF6MCr0cX4vIzJE5qyCdmSNWlM3pkZhiCcwk130_publicationInfo; a np:Nanopublication . dgn-np:NP1190648.RArfS1-vMbF6MCr0cX4vIzJE5qyCdmSNWlM3pkZhiCcwk130_assertion a np:Assertion . dgn-np:NP1190648.RArfS1-vMbF6MCr0cX4vIzJE5qyCdmSNWlM3pkZhiCcwk130_provenance a np:Provenance . dgn-np:NP1190648.RArfS1-vMbF6MCr0cX4vIzJE5qyCdmSNWlM3pkZhiCcwk130_publicationInfo a np:PublicationInfo . } dgn-np:NP1190648.RArfS1-vMbF6MCr0cX4vIzJE5qyCdmSNWlM3pkZhiCcwk130_assertion { miriam-gene:847 a ncit:C16612 . lld:C0042900 a ncit:C7057 . dgn-gda:DGN8aa6d926e7e96b01a8222fa99a801dcf sio:SIO_000628 miriam-gene:847, lld:C0042900; a sio:SIO_001121 . } dgn-np:NP1190648.RArfS1-vMbF6MCr0cX4vIzJE5qyCdmSNWlM3pkZhiCcwk130_provenance { dgn-np:NP1190648.RArfS1-vMbF6MCr0cX4vIzJE5qyCdmSNWlM3pkZhiCcwk130_assertion dcterms:description "[In conclusion, the enhanced oxidative stress with the lack of association between CAT and COMT polymorphisms and susceptibility to vitiligo in our patients suggest that mutations in other genes related to the oxidative pathway might contribute to the etiology of generalized vitiligo in Egyptian population.]. 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:24915010; 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:NP1190648.RArfS1-vMbF6MCr0cX4vIzJE5qyCdmSNWlM3pkZhiCcwk130_publicationInfo { this: dcterms:created "2016-05-13T12:50:45+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" . }