Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_assertion> ?p ?o ?g. }
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- NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_assertion type Assertion NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_head.
- NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_assertion description "[Increased incidence of p53 gene aberrations or chromosome 17p monosomy resulting from an isochromosome 17q [i(17q)] has been observed with transition of chronic myelogenous leukemia (CML) to myeloid blast crisis (BC), and in some patients with poor risk acute myeloid leukemia (AML) progressing from myelodysplastic syndrome (MDS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_provenance.
- NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_assertion evidence source_evidence_literature NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_provenance.
- NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_assertion SIO_000772 8505851 NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_provenance.
- NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_assertion wasDerivedFrom befree-2016 NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_provenance.
- NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_assertion wasGeneratedBy ECO_0000203 NP1343575.RAgw2ibe3CG_YrUfj1L0oc0lDcXtMcJvzy2Pa6CmlMYb0130_provenance.