@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:NP328853.RAoJDNIbqFuevkswhd6DTcWl3TFsZKvDP6Wu1931kc1SE130_head { this: np:hasAssertion dgn-np:NP328853.RAoJDNIbqFuevkswhd6DTcWl3TFsZKvDP6Wu1931kc1SE130_assertion; np:hasProvenance dgn-np:NP328853.RAoJDNIbqFuevkswhd6DTcWl3TFsZKvDP6Wu1931kc1SE130_provenance; np:hasPublicationInfo dgn-np:NP328853.RAoJDNIbqFuevkswhd6DTcWl3TFsZKvDP6Wu1931kc1SE130_publicationInfo; a np:Nanopublication . dgn-np:NP328853.RAoJDNIbqFuevkswhd6DTcWl3TFsZKvDP6Wu1931kc1SE130_assertion a np:Assertion . dgn-np:NP328853.RAoJDNIbqFuevkswhd6DTcWl3TFsZKvDP6Wu1931kc1SE130_provenance a np:Provenance . dgn-np:NP328853.RAoJDNIbqFuevkswhd6DTcWl3TFsZKvDP6Wu1931kc1SE130_publicationInfo a np:PublicationInfo . } dgn-np:NP328853.RAoJDNIbqFuevkswhd6DTcWl3TFsZKvDP6Wu1931kc1SE130_assertion { miriam-gene:1786 a ncit:C16612 . lld:C1140680 a ncit:C7057 . dgn-gda:DGN0e82e7962e78909e89bf32abec6dc762 sio:SIO_000628 miriam-gene:1786, lld:C1140680; a sio:SIO_001121 . } dgn-np:NP328853.RAoJDNIbqFuevkswhd6DTcWl3TFsZKvDP6Wu1931kc1SE130_provenance { dgn-np:NP328853.RAoJDNIbqFuevkswhd6DTcWl3TFsZKvDP6Wu1931kc1SE130_assertion dcterms:description "[However, based on the lack of aberrant DNMT expression in some of the cancer cell lines examined, we further suggest that another mechanism(s), in addition to DNMT overexpression, accounts for methylation anomalies commonly observed in ovarian cancer.]. 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:11531283; 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:NP328853.RAoJDNIbqFuevkswhd6DTcWl3TFsZKvDP6Wu1931kc1SE130_publicationInfo { this: dcterms:created "2016-05-13T12:44:14+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" . }