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- source_evidence_literature type ECO_0000212 NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_provenance.
- NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_assertion description "[Mutations in the genes encoding the interacting proteins AML1 and CBFbeta are the most common genetic abnormalities in acute leukaemia, and congenital mutations in the related AML3 gene are associated with disorders of osteogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_provenance.
- NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_assertion evidence source_evidence_literature NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_provenance.
- NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_assertion SIO_000772 10856244 NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_provenance.
- NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_assertion wasDerivedFrom befree-20150227 NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_provenance.
- NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_assertion wasGeneratedBy ECO_0000203 NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_provenance.
- befree-20150227 importedOn "2015-02-27" NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_provenance.