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- source_evidence_literature type ECO_0000212 NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_provenance.
- NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_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." NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_provenance.
- NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_assertion evidence source_evidence_literature NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_provenance.
- NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_assertion SIO_000772 20428194 NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_provenance.
- NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_assertion wasDerivedFrom befree-20150227 NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_provenance.
- NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_assertion wasGeneratedBy ECO_0000203 NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914091.RA4hV3Mu_axCiW9Pm9h7pG19foFFpuaMinflSbfsEhxuA130_provenance.