@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:NP900082.RAjTDU1vytsupAaMx1G-Mbme1FwGbju5BMLAKqF2p5nOc130_head { this: np:hasAssertion dgn-np:NP900082.RAjTDU1vytsupAaMx1G-Mbme1FwGbju5BMLAKqF2p5nOc130_assertion; np:hasProvenance dgn-np:NP900082.RAjTDU1vytsupAaMx1G-Mbme1FwGbju5BMLAKqF2p5nOc130_provenance; np:hasPublicationInfo dgn-np:NP900082.RAjTDU1vytsupAaMx1G-Mbme1FwGbju5BMLAKqF2p5nOc130_publicationInfo; a np:Nanopublication . dgn-np:NP900082.RAjTDU1vytsupAaMx1G-Mbme1FwGbju5BMLAKqF2p5nOc130_assertion a np:Assertion . dgn-np:NP900082.RAjTDU1vytsupAaMx1G-Mbme1FwGbju5BMLAKqF2p5nOc130_provenance a np:Provenance . dgn-np:NP900082.RAjTDU1vytsupAaMx1G-Mbme1FwGbju5BMLAKqF2p5nOc130_publicationInfo a np:PublicationInfo . } dgn-np:NP900082.RAjTDU1vytsupAaMx1G-Mbme1FwGbju5BMLAKqF2p5nOc130_assertion { miriam-gene:617 a ncit:C16612 . lld:C2745900 a ncit:C7057 . dgn-gda:DGN903077fa4b547eecaebf82e6a251d2eb sio:SIO_000628 miriam-gene:617, lld:C2745900; a sio:SIO_001121 . } dgn-np:NP900082.RAjTDU1vytsupAaMx1G-Mbme1FwGbju5BMLAKqF2p5nOc130_provenance { dgn-np:NP900082.RAjTDU1vytsupAaMx1G-Mbme1FwGbju5BMLAKqF2p5nOc130_assertion dcterms:description "[Based on Cox regression and Kaplan-Meier analyses, 5 distinct prognostic subgroups were identified: (1) very favorable: PML-RARA rearrangement (n = 29) or CEPBA double mutations (n = 42; overall survival [OS] at 3 years: 82.9%); (2) favorable: RUNX1-RUNX1T1 (n = 35), CBFB-MYH11 (n = 31), or NPM1 mutation without FLT3-ITD (n = 186; OS at 3 years: 62.6%); (3) intermediate: none of the mutations leading to assignment into groups 1, 2, 4, or 5 (n = 235; OS at 3 years: 44.2%); (4) unfavorable: MLL-PTD and/or RUNX1 mutation and/or ASXL1 mutation (n = 203; OS at 3 years: 21.9%); and (5) very unfavorable: TP53 mutation (n = 80; OS at 3 years: 0%; P < .001).]. 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:22915647; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP900082.RAjTDU1vytsupAaMx1G-Mbme1FwGbju5BMLAKqF2p5nOc130_publicationInfo { this: dcterms:created "2014-10-02T12:41:13+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }