Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_provenance.
- NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_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." NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_provenance.
- NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_assertion evidence source_evidence_literature NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_provenance.
- NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_assertion SIO_000772 16645213 NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_provenance.
- NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_assertion wasDerivedFrom befree-2016 NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_provenance.
- NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_assertion wasGeneratedBy ECO_0000203 NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_provenance.
- befree-2016 importedOn "2016-02-19" NP547269.RAwIhCZ0EVe7CGq4eO5bLKTRi2bCxzJCa8HvLQAY8ScEM130_provenance.