Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP785880.RAibHmi4skW3qMJtr7PXcf3-4O_0J0Y3foJCGh5etTb8Q130_provenance.