@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:NP1091700.RAiKLJ0v__AHawSG77nyqhP6N7GraN6Tgdv1kXzJRN8Ww130_head { this: np:hasAssertion dgn-np:NP1091700.RAiKLJ0v__AHawSG77nyqhP6N7GraN6Tgdv1kXzJRN8Ww130_assertion; np:hasProvenance dgn-np:NP1091700.RAiKLJ0v__AHawSG77nyqhP6N7GraN6Tgdv1kXzJRN8Ww130_provenance; np:hasPublicationInfo dgn-np:NP1091700.RAiKLJ0v__AHawSG77nyqhP6N7GraN6Tgdv1kXzJRN8Ww130_publicationInfo; a np:Nanopublication . dgn-np:NP1091700.RAiKLJ0v__AHawSG77nyqhP6N7GraN6Tgdv1kXzJRN8Ww130_assertion a np:Assertion . dgn-np:NP1091700.RAiKLJ0v__AHawSG77nyqhP6N7GraN6Tgdv1kXzJRN8Ww130_provenance a np:Provenance . dgn-np:NP1091700.RAiKLJ0v__AHawSG77nyqhP6N7GraN6Tgdv1kXzJRN8Ww130_publicationInfo a np:PublicationInfo . } dgn-np:NP1091700.RAiKLJ0v__AHawSG77nyqhP6N7GraN6Tgdv1kXzJRN8Ww130_assertion { miriam-gene:1356 a ncit:C16612 . lld:C0019202 a ncit:C7057 . dgn-gda:DGN76e87fd20506d34e83c65b4e45f8202c sio:SIO_000628 miriam-gene:1356, lld:C0019202; a sio:SIO_001121 . } dgn-np:NP1091700.RAiKLJ0v__AHawSG77nyqhP6N7GraN6Tgdv1kXzJRN8Ww130_provenance { dgn-np:NP1091700.RAiKLJ0v__AHawSG77nyqhP6N7GraN6Tgdv1kXzJRN8Ww130_assertion dcterms:description "[Furthermore, studies of serum copper and ceruloplasmin levels in unaffected relatives suggest that phenotypic variability in WD may be due in part to an interaction of the WND locus with other genetic or non-genetic modifiers such as age.]. 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:2382969; 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:NP1091700.RAiKLJ0v__AHawSG77nyqhP6N7GraN6Tgdv1kXzJRN8Ww130_publicationInfo { this: dcterms:created "2016-05-13T12:50:01+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" . }