Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP412235.RAiIEw9rO3JUD_anioaVbg7fecW4kl1ZvOHYpo16bZm-8#assertion> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- assertion wasGeneratedBy ECO_0000203 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion SIO_000772 10341296 provenance.
- assertion evidence source_evidence_literature provenance.
- assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.