Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_assertion type Assertion NP843716.RAP634eNNtETPe2CNWvYlGDGvxz9szJMXR-nxbzGkRfnM130_head.
- 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.