Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_assertion> ?p ?o ?g. }
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- NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_assertion type Assertion NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_head.
- NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_assertion description "[The incidence of TET2, ASXL1, CBL, IDH or IKZF1 mutations in these disorders ranges from 0 to 17%; these latter mutations are more common in chronic (TET2, ASXL1, CBL) or juvenile (CBL) myelomonocytic leukemias, mastocytosis (TET2), myelodysplastic syndromes (TET2, ASXL1) and secondary acute myeloid leukemia, including blast-phase MPN (IDH, ASXL1, IKZF1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_provenance.
- NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_assertion evidence source_evidence_literature NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_provenance.
- NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_assertion SIO_000772 20428194 NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_provenance.
- NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_assertion wasDerivedFrom befree-2016 NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_provenance.
- NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_assertion wasGeneratedBy ECO_0000203 NP809042.RApgei5A1gmMbqOyEXHdKQl894wxqTv_rQyBipLBhGH7U130_provenance.