Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_assertion> ?p ?o ?g. }
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- NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_assertion type Assertion NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_head.
- NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_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." NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_provenance.
- NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_assertion evidence source_evidence_literature NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_provenance.
- NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_assertion SIO_000772 16645213 NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_provenance.
- NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_assertion wasDerivedFrom befree-20150227 NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_provenance.
- NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_assertion wasGeneratedBy ECO_0000203 NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_provenance.