Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_provenance.
- NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_assertion description "[Fragile X syndrome (FXS) mental retardation is caused by loss-of-function mutations in an RNA-binding protein, fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_provenance.
- NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_assertion evidence source_evidence_literature NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_provenance.
- NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_assertion SIO_000772 18272470 NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_provenance.
- NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_assertion wasDerivedFrom befree-20140225 NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_provenance.
- NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_assertion wasGeneratedBy ECO_0000203 NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_provenance.