@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:NP339529.RABet3VZ6IKL0P5_QaoMSlafHbfqpNNpn_sxYqVc8dODg130_head { this: np:hasAssertion dgn-np:NP339529.RABet3VZ6IKL0P5_QaoMSlafHbfqpNNpn_sxYqVc8dODg130_assertion; np:hasProvenance dgn-np:NP339529.RABet3VZ6IKL0P5_QaoMSlafHbfqpNNpn_sxYqVc8dODg130_provenance; np:hasPublicationInfo dgn-np:NP339529.RABet3VZ6IKL0P5_QaoMSlafHbfqpNNpn_sxYqVc8dODg130_publicationInfo; a np:Nanopublication . dgn-np:NP339529.RABet3VZ6IKL0P5_QaoMSlafHbfqpNNpn_sxYqVc8dODg130_assertion a np:Assertion . dgn-np:NP339529.RABet3VZ6IKL0P5_QaoMSlafHbfqpNNpn_sxYqVc8dODg130_provenance a np:Provenance . dgn-np:NP339529.RABet3VZ6IKL0P5_QaoMSlafHbfqpNNpn_sxYqVc8dODg130_publicationInfo a np:PublicationInfo . } dgn-np:NP339529.RABet3VZ6IKL0P5_QaoMSlafHbfqpNNpn_sxYqVc8dODg130_assertion { miriam-gene:2950 a ncit:C16612 . lld:C0596263 a ncit:C7057 . dgn-gda:DGN65136b62f751ecd6bb8f43f5a9d3326d sio:SIO_000628 miriam-gene:2950, lld:C0596263; a sio:SIO_001121 . } dgn-np:NP339529.RABet3VZ6IKL0P5_QaoMSlafHbfqpNNpn_sxYqVc8dODg130_provenance { dgn-np:NP339529.RABet3VZ6IKL0P5_QaoMSlafHbfqpNNpn_sxYqVc8dODg130_assertion dcterms:description "[Human prostate cancer (PCA) cells characteristically contain hypermethylated CpG island sequences encompassing the transcriptional regulatory region of GSTP1, the gene encoding the pi-class glutathione S-transferase (GSTP1), and fail to express GSTP1 as a consequence of transcriptional silencing. Inactivation of GSTP1 by CpG island hypermethylation, the most common somatic genome alteration yet reported for human PCAs, occurs early during human prostatic carcinogenesis and results in a loss of GSTP1 caretaker function, leaving prostate cells with inadequate defenses against oxidant and electrophile carcinogens.]. 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:11751372; 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:NP339529.RABet3VZ6IKL0P5_QaoMSlafHbfqpNNpn_sxYqVc8dODg130_publicationInfo { this: dcterms:created "2016-05-13T12:44:19+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" . }