Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_provenance.
- NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_assertion description "[RUNX1 mutations clustered in the intermediate-risk cytogenetic group (46 of 640, 7.2%; cytogenetically normal, 34 of 538, 6.3%), whereas they were less frequent in adverse-risk cytogenetics (five of 109, 4.6%) and absent in core-binding-factor AML (0 of 77) and acute promyelocytic leukemia (0 of 61).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_provenance.
- NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_assertion evidence source_evidence_literature NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_provenance.
- NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_assertion SIO_000772 21343560 NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_provenance.
- NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_assertion wasDerivedFrom befree-20150227 NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_provenance.
- NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_assertion wasGeneratedBy ECO_0000203 NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285069.RApdoz5rFOgTmSiQ5ijI0w5vluawa_0e5Md4WyOUYzovM130_provenance.