Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_provenance.
- NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_assertion description "[Mutation/deletion involving FLT3 D835 are found in more than 20% of cases with MLL intragenic abnormalities compared with 10% of AML with MLL translocation and 5% of adult AML with normal MLL status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_provenance.
- NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_assertion evidence source_evidence_literature NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_provenance.
- NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_assertion SIO_000772 12791658 NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_provenance.
- NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_assertion wasDerivedFrom befree-2016 NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_provenance.
- NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_assertion wasGeneratedBy ECO_0000203 NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_provenance.
- befree-2016 importedOn "2016-02-19" NP397191.RAEJowkAAZBE0dhH0zerGwUnp1k6rJK-FTGShdHc7HWGc130_provenance.