@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:NP1004286.RAMXClP1gt6fju08PWhpkf-hSumUQfOaG1WFvnd7GIF9U130_head { this: np:hasAssertion dgn-np:NP1004286.RAMXClP1gt6fju08PWhpkf-hSumUQfOaG1WFvnd7GIF9U130_assertion; np:hasProvenance dgn-np:NP1004286.RAMXClP1gt6fju08PWhpkf-hSumUQfOaG1WFvnd7GIF9U130_provenance; np:hasPublicationInfo dgn-np:NP1004286.RAMXClP1gt6fju08PWhpkf-hSumUQfOaG1WFvnd7GIF9U130_publicationInfo; a np:Nanopublication . dgn-np:NP1004286.RAMXClP1gt6fju08PWhpkf-hSumUQfOaG1WFvnd7GIF9U130_assertion a np:Assertion . dgn-np:NP1004286.RAMXClP1gt6fju08PWhpkf-hSumUQfOaG1WFvnd7GIF9U130_provenance a np:Provenance . dgn-np:NP1004286.RAMXClP1gt6fju08PWhpkf-hSumUQfOaG1WFvnd7GIF9U130_publicationInfo a np:PublicationInfo . } dgn-np:NP1004286.RAMXClP1gt6fju08PWhpkf-hSumUQfOaG1WFvnd7GIF9U130_assertion { miriam-gene:619501 a ncit:C16612 . lld:C0008626 a ncit:C7057 . dgn-gda:DGNb19571774c65b2ea76c0d82b1fa9b0d3 sio:SIO_000628 miriam-gene:619501, lld:C0008626; a sio:SIO_001121 . } dgn-np:NP1004286.RAMXClP1gt6fju08PWhpkf-hSumUQfOaG1WFvnd7GIF9U130_provenance { dgn-np:NP1004286.RAMXClP1gt6fju08PWhpkf-hSumUQfOaG1WFvnd7GIF9U130_assertion dcterms:description "[This study represents the first analysis of primary liver cancers by CGH, and it confirms the presence of previously known chromosomal aberrations in HCC and highlights new quantitative abnormalities and sequence amplifications.]. 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:8993981; 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:NP1004286.RAMXClP1gt6fju08PWhpkf-hSumUQfOaG1WFvnd7GIF9U130_publicationInfo { this: dcterms:created "2015-08-25T14:48:02+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" . }