@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:NP435915.RA_il0VT0Z_AYJxXv6_QmxnIxKn-CfFzKVxbHHJCfLzhM130_head { this: np:hasAssertion dgn-np:NP435915.RA_il0VT0Z_AYJxXv6_QmxnIxKn-CfFzKVxbHHJCfLzhM130_assertion; np:hasProvenance dgn-np:NP435915.RA_il0VT0Z_AYJxXv6_QmxnIxKn-CfFzKVxbHHJCfLzhM130_provenance; np:hasPublicationInfo dgn-np:NP435915.RA_il0VT0Z_AYJxXv6_QmxnIxKn-CfFzKVxbHHJCfLzhM130_publicationInfo; a np:Nanopublication . dgn-np:NP435915.RA_il0VT0Z_AYJxXv6_QmxnIxKn-CfFzKVxbHHJCfLzhM130_assertion a np:Assertion . dgn-np:NP435915.RA_il0VT0Z_AYJxXv6_QmxnIxKn-CfFzKVxbHHJCfLzhM130_provenance a np:Provenance . dgn-np:NP435915.RA_il0VT0Z_AYJxXv6_QmxnIxKn-CfFzKVxbHHJCfLzhM130_publicationInfo a np:PublicationInfo . } dgn-np:NP435915.RA_il0VT0Z_AYJxXv6_QmxnIxKn-CfFzKVxbHHJCfLzhM130_assertion { miriam-gene:51343 a ncit:C16612 . lld:C0376358 a ncit:C7057 . dgn-gda:DGN79c4066123b897a4183d9d065d70df90 sio:SIO_000628 miriam-gene:51343, lld:C0376358; a sio:SIO_001121 . } dgn-np:NP435915.RA_il0VT0Z_AYJxXv6_QmxnIxKn-CfFzKVxbHHJCfLzhM130_provenance { dgn-np:NP435915.RA_il0VT0Z_AYJxXv6_QmxnIxKn-CfFzKVxbHHJCfLzhM130_assertion dcterms:description "[We found that CpG islands at GSTP1, APC, RASSF1a, PTGS2, and MDR1 were hypermethylated in >85% of prostate cancers and cancer cell lines but not in normal prostate cells and tissues; CpG islands at EDNRB, ESR1, CDKN2a, and hMLH1 exhibited low to moderate rates of hypermethylation in prostate cancer tissues and cancer cell lines but were entirely unmethylated in normal tissues; and CpG islands at DAPK1, TIMP3, MGMT, CDKN2b, p14/ARF, and CDH1 were not abnormally hypermethylated in prostate cancers.]. 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:15026333; 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:NP435915.RA_il0VT0Z_AYJxXv6_QmxnIxKn-CfFzKVxbHHJCfLzhM130_publicationInfo { this: dcterms:created "2016-05-13T12:45:03+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" . }