@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:NP1140847.RAmf_GxlNGdmpiKmdLU9atNB_Milppy4gsA4XZj4jl58A130_head { this: np:hasAssertion dgn-np:NP1140847.RAmf_GxlNGdmpiKmdLU9atNB_Milppy4gsA4XZj4jl58A130_assertion; np:hasProvenance dgn-np:NP1140847.RAmf_GxlNGdmpiKmdLU9atNB_Milppy4gsA4XZj4jl58A130_provenance; np:hasPublicationInfo dgn-np:NP1140847.RAmf_GxlNGdmpiKmdLU9atNB_Milppy4gsA4XZj4jl58A130_publicationInfo; a np:Nanopublication . dgn-np:NP1140847.RAmf_GxlNGdmpiKmdLU9atNB_Milppy4gsA4XZj4jl58A130_assertion a np:Assertion . dgn-np:NP1140847.RAmf_GxlNGdmpiKmdLU9atNB_Milppy4gsA4XZj4jl58A130_provenance a np:Provenance . dgn-np:NP1140847.RAmf_GxlNGdmpiKmdLU9atNB_Milppy4gsA4XZj4jl58A130_publicationInfo a np:PublicationInfo . } dgn-np:NP1140847.RAmf_GxlNGdmpiKmdLU9atNB_Milppy4gsA4XZj4jl58A130_assertion { miriam-gene:619501 a ncit:C16612 . lld:C2239176 a ncit:C7057 . dgn-gda:DGN71b5a6076327530874c0e324da03aaa2 sio:SIO_000628 miriam-gene:619501, lld:C2239176; a sio:SIO_001121 . } dgn-np:NP1140847.RAmf_GxlNGdmpiKmdLU9atNB_Milppy4gsA4XZj4jl58A130_provenance { dgn-np:NP1140847.RAmf_GxlNGdmpiKmdLU9atNB_Milppy4gsA4XZj4jl58A130_assertion dcterms:description "[Moreover, integration of CNAs with other high-throughput genomic data, such as aberrantly coding transcriptomes and non-coding gene expression in human HCC tissues and rodent HCC models, provides lines of evidence that can be used to facilitate the identification of novel HCC target genes with the potential of improving the survival of HCC patients.]. 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:24379610; 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:NP1140847.RAmf_GxlNGdmpiKmdLU9atNB_Milppy4gsA4XZj4jl58A130_publicationInfo { this: dcterms:created "2016-05-13T12:50:23+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" . }