@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:NP641695.RANYNbuRxsj5WKUGmyeIEP3U5aPq6L1PcJB_bsXqgFOaU130_head { this: np:hasAssertion dgn-np:NP641695.RANYNbuRxsj5WKUGmyeIEP3U5aPq6L1PcJB_bsXqgFOaU130_assertion; np:hasProvenance dgn-np:NP641695.RANYNbuRxsj5WKUGmyeIEP3U5aPq6L1PcJB_bsXqgFOaU130_provenance; np:hasPublicationInfo dgn-np:NP641695.RANYNbuRxsj5WKUGmyeIEP3U5aPq6L1PcJB_bsXqgFOaU130_publicationInfo; a np:Nanopublication . dgn-np:NP641695.RANYNbuRxsj5WKUGmyeIEP3U5aPq6L1PcJB_bsXqgFOaU130_assertion a np:Assertion . dgn-np:NP641695.RANYNbuRxsj5WKUGmyeIEP3U5aPq6L1PcJB_bsXqgFOaU130_provenance a np:Provenance . dgn-np:NP641695.RANYNbuRxsj5WKUGmyeIEP3U5aPq6L1PcJB_bsXqgFOaU130_publicationInfo a np:PublicationInfo . } dgn-np:NP641695.RANYNbuRxsj5WKUGmyeIEP3U5aPq6L1PcJB_bsXqgFOaU130_assertion { miriam-gene:595 a ncit:C16612 . lld:C0023449 a ncit:C7057 . dgn-gda:DGNd7011c00def7e698588b7610ef94ee33 sio:SIO_000628 miriam-gene:595, lld:C0023449; a sio:SIO_001121 . } dgn-np:NP641695.RANYNbuRxsj5WKUGmyeIEP3U5aPq6L1PcJB_bsXqgFOaU130_provenance { dgn-np:NP641695.RANYNbuRxsj5WKUGmyeIEP3U5aPq6L1PcJB_bsXqgFOaU130_assertion dcterms:description "[We have demonstrated that WNT5A, a putative tumour suppressor gene in ALL, is silenced by methylation in this disease and that this epigenetic event is associated with upregulation of CYCLIN D1 expression and confers poor prognosis in this group of 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:18032022; 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:NP641695.RANYNbuRxsj5WKUGmyeIEP3U5aPq6L1PcJB_bsXqgFOaU130_publicationInfo { this: dcterms:created "2016-05-13T12:46:36+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" . }