@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:NP306723.RAn_-2TyGQPfURVJot2z-JaWU_IfL-xUwxnUE9ODurYfg130_head { this: np:hasAssertion dgn-np:NP306723.RAn_-2TyGQPfURVJot2z-JaWU_IfL-xUwxnUE9ODurYfg130_assertion; np:hasProvenance dgn-np:NP306723.RAn_-2TyGQPfURVJot2z-JaWU_IfL-xUwxnUE9ODurYfg130_provenance; np:hasPublicationInfo dgn-np:NP306723.RAn_-2TyGQPfURVJot2z-JaWU_IfL-xUwxnUE9ODurYfg130_publicationInfo; a np:Nanopublication . dgn-np:NP306723.RAn_-2TyGQPfURVJot2z-JaWU_IfL-xUwxnUE9ODurYfg130_assertion a np:Assertion . dgn-np:NP306723.RAn_-2TyGQPfURVJot2z-JaWU_IfL-xUwxnUE9ODurYfg130_provenance a np:Provenance . dgn-np:NP306723.RAn_-2TyGQPfURVJot2z-JaWU_IfL-xUwxnUE9ODurYfg130_publicationInfo a np:PublicationInfo . } dgn-np:NP306723.RAn_-2TyGQPfURVJot2z-JaWU_IfL-xUwxnUE9ODurYfg130_assertion { miriam-gene:1029 a ncit:C16612 . lld:C1516669 a ncit:C7057 . dgn-gda:DGNb7158c230cb1c1d3fbd737d94950890f sio:SIO_000628 miriam-gene:1029, lld:C1516669; a sio:SIO_001121 . } dgn-np:NP306723.RAn_-2TyGQPfURVJot2z-JaWU_IfL-xUwxnUE9ODurYfg130_provenance { dgn-np:NP306723.RAn_-2TyGQPfURVJot2z-JaWU_IfL-xUwxnUE9ODurYfg130_assertion dcterms:description "[These data: (i) point to a back-up 'senescence' mechanism distinct from induction of p21(Waf1) or p16(Ink4a); and (ii) provide an in vitro model of clonal evolution through successive dysfunction of Rb and p53 pathways in a relevant human cell context.]. 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:12082615; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP306723.RAn_-2TyGQPfURVJot2z-JaWU_IfL-xUwxnUE9ODurYfg130_publicationInfo { this: dcterms:created "2015-08-25T14:40:36+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }