Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_provenance.
- NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_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." NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_provenance.
- NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_assertion evidence source_evidence_literature NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_provenance.
- NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_assertion SIO_000772 20428194 NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_provenance.
- NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_assertion wasDerivedFrom befree-20150227 NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_provenance.
- NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_assertion wasGeneratedBy ECO_0000203 NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978615.RA1rgOQepOWCd7a5oM3eXjrdMloTX1j4ZEWar3FFX9F10130_provenance.