Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_assertion> ?p ?o ?g. }
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- NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_assertion type Assertion NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_head.
- NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_provenance.
- NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_assertion evidence source_evidence_literature NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_provenance.
- NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_assertion SIO_000772 7585014 NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_provenance.
- NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_assertion wasDerivedFrom befree-20140225 NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_provenance.
- NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_assertion wasGeneratedBy ECO_0000203 NP885577.RAYmAk4WzIbqHjvVZZXWwyCK27kOI7gyZt0cXvtuOs96o130_provenance.