Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_provenance.
- NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_assertion description "[High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_provenance.
- NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_assertion evidence source_evidence_literature NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_provenance.
- NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_assertion SIO_000772 16646086 NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_provenance.
- NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_assertion wasDerivedFrom befree-20140225 NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_provenance.
- NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_assertion wasGeneratedBy ECO_0000203 NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477960.RAkNAFHjKW8pnEDNfBh31K13AKAClQDEeunFNfvpz1egw130_provenance.