@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:NP1264965.RAWZofSUvp5F8rC_GuZToyyE6tiIGM_b5XpgLA6akBJaY130_head { this: np:hasAssertion dgn-np:NP1264965.RAWZofSUvp5F8rC_GuZToyyE6tiIGM_b5XpgLA6akBJaY130_assertion; np:hasProvenance dgn-np:NP1264965.RAWZofSUvp5F8rC_GuZToyyE6tiIGM_b5XpgLA6akBJaY130_provenance; np:hasPublicationInfo dgn-np:NP1264965.RAWZofSUvp5F8rC_GuZToyyE6tiIGM_b5XpgLA6akBJaY130_publicationInfo; a np:Nanopublication . dgn-np:NP1264965.RAWZofSUvp5F8rC_GuZToyyE6tiIGM_b5XpgLA6akBJaY130_assertion a np:Assertion . dgn-np:NP1264965.RAWZofSUvp5F8rC_GuZToyyE6tiIGM_b5XpgLA6akBJaY130_provenance a np:Provenance . dgn-np:NP1264965.RAWZofSUvp5F8rC_GuZToyyE6tiIGM_b5XpgLA6akBJaY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1264965.RAWZofSUvp5F8rC_GuZToyyE6tiIGM_b5XpgLA6akBJaY130_assertion { miriam-gene:10992 a ncit:C16612 . lld:C0677932 a ncit:C7057 . dgn-gda:DGN45a16f916809e01bbcdaddee66150fc1 sio:SIO_000628 miriam-gene:10992, lld:C0677932; a sio:SIO_001121 . } dgn-np:NP1264965.RAWZofSUvp5F8rC_GuZToyyE6tiIGM_b5XpgLA6akBJaY130_provenance { dgn-np:NP1264965.RAWZofSUvp5F8rC_GuZToyyE6tiIGM_b5XpgLA6akBJaY130_assertion dcterms:description "[Acquired defects in the p53 pathway, activating mutations of NOTCH1, and dysfunctional mutations of SF3B1 and BIRC3 identify patients with higher risk of progressive disease, poorer responses to conventional chemoimmunotherapy, and shorter survival.]. 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:25696844; 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:NP1264965.RAWZofSUvp5F8rC_GuZToyyE6tiIGM_b5XpgLA6akBJaY130_publicationInfo { this: dcterms:created "2016-05-13T12:51:19+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" . }