@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:NP466446.RAWAK2YYV2QvM2TQsITfJ_GguN9VkKsIVxxxyXKn-Vdys130_head { this: np:hasAssertion dgn-np:NP466446.RAWAK2YYV2QvM2TQsITfJ_GguN9VkKsIVxxxyXKn-Vdys130_assertion; np:hasProvenance dgn-np:NP466446.RAWAK2YYV2QvM2TQsITfJ_GguN9VkKsIVxxxyXKn-Vdys130_provenance; np:hasPublicationInfo dgn-np:NP466446.RAWAK2YYV2QvM2TQsITfJ_GguN9VkKsIVxxxyXKn-Vdys130_publicationInfo; a np:Nanopublication . dgn-np:NP466446.RAWAK2YYV2QvM2TQsITfJ_GguN9VkKsIVxxxyXKn-Vdys130_assertion a np:Assertion . dgn-np:NP466446.RAWAK2YYV2QvM2TQsITfJ_GguN9VkKsIVxxxyXKn-Vdys130_provenance a np:Provenance . dgn-np:NP466446.RAWAK2YYV2QvM2TQsITfJ_GguN9VkKsIVxxxyXKn-Vdys130_publicationInfo a np:PublicationInfo . } dgn-np:NP466446.RAWAK2YYV2QvM2TQsITfJ_GguN9VkKsIVxxxyXKn-Vdys130_assertion { miriam-gene:540 a ncit:C16612 . lld:C0019202 a ncit:C7057 . dgn-gda:DGN8cc48787aa80d643274e513a861a3768 sio:SIO_000628 miriam-gene:540, lld:C0019202; a sio:SIO_001121 . } dgn-np:NP466446.RAWAK2YYV2QvM2TQsITfJ_GguN9VkKsIVxxxyXKn-Vdys130_provenance { dgn-np:NP466446.RAWAK2YYV2QvM2TQsITfJ_GguN9VkKsIVxxxyXKn-Vdys130_assertion dcterms:description "[These results indicated that the human ATP7B product compensated for the deficiency of the endogenous rattus protein and did function in intrahepatic copper transport by secreting copper into the plasma via incorporation into ceruloplasmin and by the excretion of copper into the bile, and that ATP7B is critical to hepatic dysfunctions in WD.]. 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:15511628; 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:NP466446.RAWAK2YYV2QvM2TQsITfJ_GguN9VkKsIVxxxyXKn-Vdys130_publicationInfo { this: dcterms:created "2016-05-13T12:45:16+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" . }