@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:NP257328.RAdRNICw2N3AxlxdSgPX7JoG4CFnm109X1chP-ZtFGgaA130_head { this: np:hasAssertion dgn-np:NP257328.RAdRNICw2N3AxlxdSgPX7JoG4CFnm109X1chP-ZtFGgaA130_assertion; np:hasProvenance dgn-np:NP257328.RAdRNICw2N3AxlxdSgPX7JoG4CFnm109X1chP-ZtFGgaA130_provenance; np:hasPublicationInfo dgn-np:NP257328.RAdRNICw2N3AxlxdSgPX7JoG4CFnm109X1chP-ZtFGgaA130_publicationInfo; a np:Nanopublication . dgn-np:NP257328.RAdRNICw2N3AxlxdSgPX7JoG4CFnm109X1chP-ZtFGgaA130_assertion a np:Assertion . dgn-np:NP257328.RAdRNICw2N3AxlxdSgPX7JoG4CFnm109X1chP-ZtFGgaA130_provenance a np:Provenance . dgn-np:NP257328.RAdRNICw2N3AxlxdSgPX7JoG4CFnm109X1chP-ZtFGgaA130_publicationInfo a np:PublicationInfo . } dgn-np:NP257328.RAdRNICw2N3AxlxdSgPX7JoG4CFnm109X1chP-ZtFGgaA130_assertion { miriam-gene:545 a ncit:C16612 . lld:C0023434 a ncit:C7057 . dgn-gda:DGN824731ac655e1026e9ae9ce45076d030 sio:SIO_000628 miriam-gene:545, lld:C0023434; a sio:SIO_001121 . } dgn-np:NP257328.RAdRNICw2N3AxlxdSgPX7JoG4CFnm109X1chP-ZtFGgaA130_provenance { dgn-np:NP257328.RAdRNICw2N3AxlxdSgPX7JoG4CFnm109X1chP-ZtFGgaA130_assertion dcterms:description "[The functional assay was set-up on cell lines recapitulating all TP53 genotypes (EHEB, TP53(wt/wt); RAJI, TP53(mut/wt); MEC-1 and MAVER1, TP53(mut/del); HL-60, TP53(del/del)) and evaluated in two multi-institutional cohorts, purposely enriched in CLL bearing TP53 disruption: a training cohort of 100 cases and a validation cohort of 40 cases, both characterized by FISH and TP53 direct sequencing.]. 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:24283248; 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:NP257328.RAdRNICw2N3AxlxdSgPX7JoG4CFnm109X1chP-ZtFGgaA130_publicationInfo { this: dcterms:created "2015-08-25T14:40:06+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" . }