Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_assertion> ?p ?o ?g. }
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- NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_assertion type Assertion NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_head.
- NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_assertion description "[NPM1 gene mutations are the most frequent genetic lesion in the 60% of adult acute myeloid leukemias (AMLs) with normal karyotype and no evidence of typical fusion genes (BCR/ABL1, PML/RARA, AML1/ETO, CBFB/MYH11, DEK/CAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_provenance.
- NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_assertion evidence source_evidence_literature NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_provenance.
- NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_assertion SIO_000772 16645213 NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_provenance.
- NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_assertion wasDerivedFrom befree-20140225 NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_provenance.
- NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_assertion wasGeneratedBy ECO_0000203 NP162668.RAZ23mqumeS1IfK2PobivEJfjwSc_XzfCCQS2OtJ1CurA130_provenance.