@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:NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_head { this: np:hasAssertion dgn-np:NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_assertion; np:hasProvenance dgn-np:NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_provenance; np:hasPublicationInfo dgn-np:NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_publicationInfo; a np:Nanopublication . dgn-np:NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_assertion a np:Assertion . dgn-np:NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_provenance a np:Provenance . dgn-np:NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_publicationInfo a np:PublicationInfo . } dgn-np:NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_assertion { miriam-gene:4297 a ncit:C16612 . lld:C0008626 a ncit:C7057 . dgn-gda:DGN2be0f4cfcee26e3be1c42646d9bf9349 sio:SIO_000628 miriam-gene:4297, lld:C0008626; a sio:SIO_001121 . } dgn-np:NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_provenance { dgn-np:NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_assertion dcterms:description "[There was a clear-cut clinical difference between the 28 patients having a balanced 11q23 anomaly/MLL rearrangement and the 17 patients having an unbalanced chromosomal anomaly: AML with unbalanced 11q23 anomalies occurred in older patients (P = 0.07) tended to be less frequently associated with previous exposure to topoisomerase II-active drugs and with M4/M5 FAB cytological subtypes, were always associated with other chromosomal anomalies (P < 0.0001), expressed more frequently the CD34 antigen (P = 0.05) and were of considerably poorer prognosis for achievement of CR (P = 0.005) and survival (P = 0.0005).]. 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:9436917; 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:NP261965.RAUmV9pOPe34QFilp1QYiIEkdeDVI1Z25gBJax4TTZIrY130_publicationInfo { this: dcterms:created "2014-10-02T12:34:26+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" . }