Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_provenance.
- NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_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." NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_provenance.
- NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_assertion evidence source_evidence_literature NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_provenance.
- NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_assertion SIO_000772 20428194 NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_provenance.
- NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_assertion wasDerivedFrom befree-2016 NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_provenance.
- NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_assertion wasGeneratedBy ECO_0000203 NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_provenance.
- befree-2016 importedOn "2016-02-19" NP809048.RAUx3dzC5R7FwPzO1Au6IRbx4TlmjjxqCxZtDi5SCaSoA130_provenance.