@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:NP1119461.RANQJTP8jyWcmW0sOESOOoOUsXAdcndml6aa-JJMN5XCM130_head { this: np:hasAssertion dgn-np:NP1119461.RANQJTP8jyWcmW0sOESOOoOUsXAdcndml6aa-JJMN5XCM130_assertion; np:hasProvenance dgn-np:NP1119461.RANQJTP8jyWcmW0sOESOOoOUsXAdcndml6aa-JJMN5XCM130_provenance; np:hasPublicationInfo dgn-np:NP1119461.RANQJTP8jyWcmW0sOESOOoOUsXAdcndml6aa-JJMN5XCM130_publicationInfo; a np:Nanopublication . dgn-np:NP1119461.RANQJTP8jyWcmW0sOESOOoOUsXAdcndml6aa-JJMN5XCM130_assertion a np:Assertion . dgn-np:NP1119461.RANQJTP8jyWcmW0sOESOOoOUsXAdcndml6aa-JJMN5XCM130_provenance a np:Provenance . dgn-np:NP1119461.RANQJTP8jyWcmW0sOESOOoOUsXAdcndml6aa-JJMN5XCM130_publicationInfo a np:PublicationInfo . } dgn-np:NP1119461.RANQJTP8jyWcmW0sOESOOoOUsXAdcndml6aa-JJMN5XCM130_assertion { miriam-gene:4851 a ncit:C16612 . lld:C0023434 a ncit:C7057 . dgn-gda:DGNbdf76469495fd04c1e6e94a079bfdd9f sio:SIO_000628 miriam-gene:4851, lld:C0023434; a sio:SIO_001121 . } dgn-np:NP1119461.RANQJTP8jyWcmW0sOESOOoOUsXAdcndml6aa-JJMN5XCM130_provenance { dgn-np:NP1119461.RANQJTP8jyWcmW0sOESOOoOUsXAdcndml6aa-JJMN5XCM130_assertion dcterms:description "[RS lesions are heterogeneous in terms of load and spectrum among patients, and include those involved in CLL progression and chemorefractoriness (TP53 disruption and NOTCH1 activation) as well as some not previously implicated in CLL or RS pathogenesis.]. 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:24127483; 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:NP1119461.RANQJTP8jyWcmW0sOESOOoOUsXAdcndml6aa-JJMN5XCM130_publicationInfo { this: dcterms:created "2016-05-13T12:50:13+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" . }