@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:NP419447.RA1u-otaPp1ZXltDkS0YpiYqLULRvgdOLV1z9jJOz2P8c130_head { this: np:hasAssertion dgn-np:NP419447.RA1u-otaPp1ZXltDkS0YpiYqLULRvgdOLV1z9jJOz2P8c130_assertion; np:hasProvenance dgn-np:NP419447.RA1u-otaPp1ZXltDkS0YpiYqLULRvgdOLV1z9jJOz2P8c130_provenance; np:hasPublicationInfo dgn-np:NP419447.RA1u-otaPp1ZXltDkS0YpiYqLULRvgdOLV1z9jJOz2P8c130_publicationInfo; a np:Nanopublication . dgn-np:NP419447.RA1u-otaPp1ZXltDkS0YpiYqLULRvgdOLV1z9jJOz2P8c130_assertion a np:Assertion . dgn-np:NP419447.RA1u-otaPp1ZXltDkS0YpiYqLULRvgdOLV1z9jJOz2P8c130_provenance a np:Provenance . dgn-np:NP419447.RA1u-otaPp1ZXltDkS0YpiYqLULRvgdOLV1z9jJOz2P8c130_publicationInfo a np:PublicationInfo . } dgn-np:NP419447.RA1u-otaPp1ZXltDkS0YpiYqLULRvgdOLV1z9jJOz2P8c130_assertion { miriam-gene:540 a ncit:C16612 . lld:C0019202 a ncit:C7057 . dgn-gda:DGNc8507fdc4ea00920cf9c5790814609d6 sio:SIO_000628 miriam-gene:540, lld:C0019202; a sio:SIO_001121 . } dgn-np:NP419447.RA1u-otaPp1ZXltDkS0YpiYqLULRvgdOLV1z9jJOz2P8c130_provenance { dgn-np:NP419447.RA1u-otaPp1ZXltDkS0YpiYqLULRvgdOLV1z9jJOz2P8c130_assertion dcterms:description "[This approach could be the method of choice to implement molecular genetic testing in clinical laboratories, even those not especially equipped for DNA analysis and in particular in newly developed molecular genetics centers in countries whose population has not yet been characterized for WD-causing ATP7B gene mutations.]. 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:14602476; 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:NP419447.RA1u-otaPp1ZXltDkS0YpiYqLULRvgdOLV1z9jJOz2P8c130_publicationInfo { this: dcterms:created "2016-05-13T12:44:55+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" . }