Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_provenance.
- NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_assertion description "[In this report, we show that AML1 point mutations were found in 26 (23.6%) of 110 patients with refractory anemia with excess blasts (RAEB), RAEB in transformation (RAEBt), and AML following MDS (defined these 3 disease categories as MDS/AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_provenance.
- NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_assertion evidence source_evidence_literature NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_provenance.
- NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_assertion SIO_000772 14615365 NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_provenance.
- NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_assertion wasDerivedFrom befree-20150227 NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_provenance.
- NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_assertion wasGeneratedBy ECO_0000203 NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP284863.RAijJWpbhrikfSADOtNi0JlB02LRAK9Rs5ibKpvw931H8130_provenance.