Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_provenance.
- NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_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." NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_provenance.
- NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_assertion evidence source_evidence_literature NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_provenance.
- NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_assertion SIO_000772 12791658 NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_provenance.
- NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_assertion wasDerivedFrom befree-20140225 NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_provenance.
- NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_assertion wasGeneratedBy ECO_0000203 NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP170794.RAYG8eUAyvzmwZKXRSu1c41xLd3eokhkYKHQ6fVzj0H7o130_provenance.