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- source_evidence_literature type ECO_0000212 NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_provenance.
- NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_assertion description "[Three patients showed extra copies of chromosome 21 including a case in which the trisomy 21 (+21) clone was distinct from the one harboring TEL/AML1 gene fusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_provenance.
- NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_assertion evidence source_evidence_literature NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_provenance.
- NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_assertion SIO_000772 11516105 NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_provenance.
- NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_assertion wasDerivedFrom befree-20140225 NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_provenance.
- NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_assertion wasGeneratedBy ECO_0000203 NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP529236.RAElpH_YE6sCXSOxY1LNX_35sFDUfTycjG6pFcogyvxdU130_provenance.