@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:NP559054.RAHtjTxgQ9OIVSSChwCGETG3zVSvPbkGrEaHPfa1osbh0130_head { this: np:hasAssertion dgn-np:NP559054.RAHtjTxgQ9OIVSSChwCGETG3zVSvPbkGrEaHPfa1osbh0130_assertion; np:hasProvenance dgn-np:NP559054.RAHtjTxgQ9OIVSSChwCGETG3zVSvPbkGrEaHPfa1osbh0130_provenance; np:hasPublicationInfo dgn-np:NP559054.RAHtjTxgQ9OIVSSChwCGETG3zVSvPbkGrEaHPfa1osbh0130_publicationInfo; a np:Nanopublication . dgn-np:NP559054.RAHtjTxgQ9OIVSSChwCGETG3zVSvPbkGrEaHPfa1osbh0130_assertion a np:Assertion . dgn-np:NP559054.RAHtjTxgQ9OIVSSChwCGETG3zVSvPbkGrEaHPfa1osbh0130_provenance a np:Provenance . dgn-np:NP559054.RAHtjTxgQ9OIVSSChwCGETG3zVSvPbkGrEaHPfa1osbh0130_publicationInfo a np:PublicationInfo . } dgn-np:NP559054.RAHtjTxgQ9OIVSSChwCGETG3zVSvPbkGrEaHPfa1osbh0130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C1140680 a ncit:C7057 . dgn-gda:DGNe2778d6dca7e5756bc988e9937b6ec94 sio:SIO_000628 miriam-gene:7157, lld:C1140680; a sio:SIO_001121 . } dgn-np:NP559054.RAHtjTxgQ9OIVSSChwCGETG3zVSvPbkGrEaHPfa1osbh0130_provenance { dgn-np:NP559054.RAHtjTxgQ9OIVSSChwCGETG3zVSvPbkGrEaHPfa1osbh0130_assertion dcterms:description "[As both p53 pathway dysfunction and activation of telomerase are commonly present in human ovarian cancer, these immortal cells provide an authetic cell model system for the study of the human ovarian cancer initiation, progression, differentiation and chemoprevention.]. 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:16829690; 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:NP559054.RAHtjTxgQ9OIVSSChwCGETG3zVSvPbkGrEaHPfa1osbh0130_publicationInfo { this: dcterms:created "2016-05-13T12:45:58+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" . }