@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:NP884182.RAf_t0KtsivQUOM97Zoxj7QIkcpM1D18u7Hsh7LoSOp0I130_head { this: np:hasAssertion dgn-np:NP884182.RAf_t0KtsivQUOM97Zoxj7QIkcpM1D18u7Hsh7LoSOp0I130_assertion; np:hasProvenance dgn-np:NP884182.RAf_t0KtsivQUOM97Zoxj7QIkcpM1D18u7Hsh7LoSOp0I130_provenance; np:hasPublicationInfo dgn-np:NP884182.RAf_t0KtsivQUOM97Zoxj7QIkcpM1D18u7Hsh7LoSOp0I130_publicationInfo; a np:Nanopublication . dgn-np:NP884182.RAf_t0KtsivQUOM97Zoxj7QIkcpM1D18u7Hsh7LoSOp0I130_assertion a np:Assertion . dgn-np:NP884182.RAf_t0KtsivQUOM97Zoxj7QIkcpM1D18u7Hsh7LoSOp0I130_provenance a np:Provenance . dgn-np:NP884182.RAf_t0KtsivQUOM97Zoxj7QIkcpM1D18u7Hsh7LoSOp0I130_publicationInfo a np:PublicationInfo . } dgn-np:NP884182.RAf_t0KtsivQUOM97Zoxj7QIkcpM1D18u7Hsh7LoSOp0I130_assertion { miriam-gene:4193 a ncit:C16612 . lld:C0027819 a ncit:C7057 . dgn-gda:DGN72228e4b5996f084dd037a53e8189191 sio:SIO_000628 miriam-gene:4193, lld:C0027819; a sio:SIO_001121 . } dgn-np:NP884182.RAf_t0KtsivQUOM97Zoxj7QIkcpM1D18u7Hsh7LoSOp0I130_provenance { dgn-np:NP884182.RAf_t0KtsivQUOM97Zoxj7QIkcpM1D18u7Hsh7LoSOp0I130_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:NP884182.RAf_t0KtsivQUOM97Zoxj7QIkcpM1D18u7Hsh7LoSOp0I130_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" . }