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- source_evidence_literature type ECO_0000212 NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_provenance.
- NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_assertion description "[One PDE11A inactivating mutation (R307X) was found in one ACA, 22 germ-line missense variants (18.8%) were found in adrenocortical tumors, and only 11 missense variants (5.7%) were found in controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_provenance.
- NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_assertion evidence source_evidence_literature NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_provenance.
- NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_assertion SIO_000772 18559625 NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_provenance.
- NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_assertion wasDerivedFrom befree-20150227 NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_provenance.
- NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_assertion wasGeneratedBy ECO_0000203 NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP899107.RAXPzg2YL-LyNAob9rAix8IzWZ7G3n6mxHojMoqha_SSo130_provenance.