Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance.
- NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_assertion description "[We genotyped ASXL1 and up to 18 other genes including epigenetic (TET2, EZH2, IDH1, IDH2, DNMT3A), splicing (SF3B1, SRSF2, ZRSF2, U2AF1), transcription (RUNX1, NPM1, TP53), and signaling (NRAS, KRAS, CBL, JAK2, FLT3) regulators in 312 patients with CMML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance.
- NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_assertion evidence source_evidence_literature NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance.
- NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_assertion SIO_000772 23690417 NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance.
- NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_assertion wasDerivedFrom befree-20140225 NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance.
- NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_assertion wasGeneratedBy ECO_0000203 NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance.