Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- 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." provenance.
- 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." provenance.
- 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." provenance.
- NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_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." NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_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.