@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:NP884183.RAY1oYeYuL_xV6SLWm6vcSm1ELnKig_BqSalhwqD3DzmQ130_head { this: np:hasAssertion dgn-np:NP884183.RAY1oYeYuL_xV6SLWm6vcSm1ELnKig_BqSalhwqD3DzmQ130_assertion; np:hasProvenance dgn-np:NP884183.RAY1oYeYuL_xV6SLWm6vcSm1ELnKig_BqSalhwqD3DzmQ130_provenance; np:hasPublicationInfo dgn-np:NP884183.RAY1oYeYuL_xV6SLWm6vcSm1ELnKig_BqSalhwqD3DzmQ130_publicationInfo; a np:Nanopublication . dgn-np:NP884183.RAY1oYeYuL_xV6SLWm6vcSm1ELnKig_BqSalhwqD3DzmQ130_assertion a np:Assertion . dgn-np:NP884183.RAY1oYeYuL_xV6SLWm6vcSm1ELnKig_BqSalhwqD3DzmQ130_provenance a np:Provenance . dgn-np:NP884183.RAY1oYeYuL_xV6SLWm6vcSm1ELnKig_BqSalhwqD3DzmQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP884183.RAY1oYeYuL_xV6SLWm6vcSm1ELnKig_BqSalhwqD3DzmQ130_assertion { miriam-gene:4193 a ncit:C16612 . lld:C0700095 a ncit:C7057 . dgn-gda:DGNe76b1448edc837fce2acc4a84b65b1a8 sio:SIO_000628 miriam-gene:4193, lld:C0700095; a sio:SIO_001121 . } dgn-np:NP884183.RAY1oYeYuL_xV6SLWm6vcSm1ELnKig_BqSalhwqD3DzmQ130_provenance { dgn-np:NP884183.RAY1oYeYuL_xV6SLWm6vcSm1ELnKig_BqSalhwqD3DzmQ130_assertion dcterms:description "[Our findings shed light on the spectrum of p53 pathway lesions in neuroblastoma cells, indicate that defects in effector molecules downstream of p53 are remarkably rare in neuroblastoma, and identify p14(ARF) as a determinant of the outcome of the response to MDM2 inhibition.]. 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:21460101; 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:NP884183.RAY1oYeYuL_xV6SLWm6vcSm1ELnKig_BqSalhwqD3DzmQ130_publicationInfo { this: dcterms:created "2016-05-13T12:48:25+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" . }