Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_provenance.
- NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_assertion wasGeneratedBy ECO_0000203 NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_provenance.
- NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_assertion wasDerivedFrom befree-20140225 NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_provenance.
- NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_assertion SIO_000772 23335386 NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_provenance.
- NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_assertion evidence source_evidence_literature NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_provenance.
- NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_assertion description "[In this study of 226 patients with chronic myelomonocytic leukemia (CMML), mutational frequencies were 40% for SRSF2 (all affecting P95), 6% for SF3B1 (primarily K700E) and 9% for U2AF35 (mostly S34F and Q157P/R).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP496447.RALIOocPs7UYrFe58uq03xgc6tQOqRFCC86dkeiXZUa0o130_provenance.