Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_provenance.
- NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_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." NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_provenance.
- NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_assertion evidence source_evidence_literature NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_provenance.
- NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_assertion SIO_000772 12791658 NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_provenance.
- NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_assertion wasDerivedFrom befree-20150227 NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_provenance.
- NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_assertion wasGeneratedBy ECO_0000203 NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP559137.RAgSgeaLM43reIdd3rQe3exys9DAXritisbgXtX7IukY0130_provenance.