Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_provenance.
- NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_assertion description "[Our study showed that MRC-AML as defined in the WHO 2008 classification presents a specific mutation pattern characterized by a high frequency of ASXL1 mutations and a low rate of NPM1, FLT3, and DNMT3A mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_provenance.
- NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_assertion evidence source_evidence_literature NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_provenance.
- NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_assertion SIO_000772 22535592 NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_provenance.
- NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_assertion wasDerivedFrom befree-2016 NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_provenance.
- NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_assertion wasGeneratedBy ECO_0000203 NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_provenance.
- befree-2016 importedOn "2016-02-19" NP977688.RASICI10dDa_R9cTjNR1C7KEFGdaclAU1lCLk2HfqQDFM130_provenance.