Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_assertion type Assertion NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_head.
- NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_assertion wasGeneratedBy ECO_0000203 NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_provenance.
- NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_assertion wasDerivedFrom befree-2016 NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_provenance.
- NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_assertion SIO_000772 9211186 NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_provenance.
- NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_assertion evidence source_evidence_literature NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_provenance.
- NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_assertion description "[The fragile X syndrome is caused by the amplification of a polymorphic CGG repeat in the 5' untranslated region of the FMR1 gene and is the most common form of inherited mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1376230.RAVtHuyPYa8oXaG4XHCrkV5dat7210qGolWGMov5ddgQE130_provenance.