Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_assertion> ?p ?o ?g. }
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- NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_assertion type Assertion NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_head.
- NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_assertion wasGeneratedBy ECO_0000203 NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_provenance.
- NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_assertion wasDerivedFrom befree-20150227 NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_provenance.
- NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_assertion SIO_000772 1450412 NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_provenance.
- NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_assertion evidence source_evidence_literature NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_provenance.
- NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_assertion description "[The overall frequency of abnormalities of chromosomes 5 and/or 7 observed in our M6 patients is similar to that observed in our patients with therapy-related acute myeloid leukemia (t-AML; 99 of 129 patients, 77%), but substantially higher than that noted in our other patients with AML de novo (French-American-British [FAB] subtypes M1-M5: 52 of 334 patients, 16%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394456.RADxlY1rZZwQdaeHst50C95xsUCR9kjufcizWudPuXFX0130_provenance.