Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_provenance.
- befree-2016 importedOn "2016-02-19" NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_provenance.
- NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_assertion wasGeneratedBy ECO_0000203 NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_provenance.
- NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_assertion wasDerivedFrom befree-2016 NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_provenance.
- NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_assertion SIO_000772 23335386 NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_provenance.
- NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_assertion evidence source_evidence_literature NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_provenance.
- NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_assertion description "[We conclude that SRSF2 is the most frequently mutated spliceosome gene in CMML but neither it nor SF3B1 or U2AF35 mutations are prognostically relevant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045434.RAWV84MReGBzE2mDb99XU0CazfXLDRqhnnLvays2oeV10130_provenance.