Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_provenance.
- NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_assertion wasGeneratedBy ECO_0000203 NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_provenance.
- NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_assertion wasDerivedFrom befree-20150227 NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_provenance.
- NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_assertion SIO_000772 24903747 NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_provenance.
- NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_assertion evidence source_evidence_literature NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_provenance.
- NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_assertion description "[Recent studies are shedding light on the molecular basis of myelodysplasia and how mutations and epimutations can induce and promote this neoplastic process through aberrant transcription factor function (RUNX1, ETV6, TP53), kinase signalling (FLT3, NRAS, KIT, CBL) and epigenetic deregulation (TET2, IDH1/2, DNMT3A, EZH2, ASXL1, SF3B1, U2AF1, SRSF2, ZRSR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914026.RAdLcBWy0p3Ac87xdK-U7ORiD6wn6ILoUwsWHOeSHzT8A130_provenance.