Matches in Nanopublications for { ?s ?p "[Spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2) and Machado-Joseph disease or spinocerebellar ataxia type 3 (MJD/SCA3) are three distinctive forms of autosomal dominant spinocerebellar ataxia (SCA) caused by expansions of an unstable CAG repeat localized in the coding region of the causative genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP557478.RACqtOZ2AMxlBqXadSPe0FxqTbXwgRU3A3jIkDjLVqbKk130_assertion description "[Spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2) and Machado-Joseph disease or spinocerebellar ataxia type 3 (MJD/SCA3) are three distinctive forms of autosomal dominant spinocerebellar ataxia (SCA) caused by expansions of an unstable CAG repeat localized in the coding region of the causative genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557478.RACqtOZ2AMxlBqXadSPe0FxqTbXwgRU3A3jIkDjLVqbKk130_provenance.
- NP1397482.RAAEGCikqpXO0SkB46JHAd56yppdyEu-2b51Y5NXeKOKo130_assertion description "[Spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2) and Machado-Joseph disease or spinocerebellar ataxia type 3 (MJD/SCA3) are three distinctive forms of autosomal dominant spinocerebellar ataxia (SCA) caused by expansions of an unstable CAG repeat localized in the coding region of the causative genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1397482.RAAEGCikqpXO0SkB46JHAd56yppdyEu-2b51Y5NXeKOKo130_provenance.
- NP1397481.RA2PLwqZ7hAmzFCJRJXeO1ePebujcZVdpmX965Ztr03DI130_assertion description "[Spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2) and Machado-Joseph disease or spinocerebellar ataxia type 3 (MJD/SCA3) are three distinctive forms of autosomal dominant spinocerebellar ataxia (SCA) caused by expansions of an unstable CAG repeat localized in the coding region of the causative genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1397481.RA2PLwqZ7hAmzFCJRJXeO1ePebujcZVdpmX965Ztr03DI130_provenance.
- NP1397483.RA3B5KkiU0PKy4TgQgQgzjSF3dWEQ6GrziXvYuLjfnHog130_assertion description "[Spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2) and Machado-Joseph disease or spinocerebellar ataxia type 3 (MJD/SCA3) are three distinctive forms of autosomal dominant spinocerebellar ataxia (SCA) caused by expansions of an unstable CAG repeat localized in the coding region of the causative genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1397483.RA3B5KkiU0PKy4TgQgQgzjSF3dWEQ6GrziXvYuLjfnHog130_provenance.
- assertion description "[Spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2) and Machado-Joseph disease or spinocerebellar ataxia type 3 (MJD/SCA3) are three distinctive forms of autosomal dominant spinocerebellar ataxia (SCA) caused by expansions of an unstable CAG repeat localized in the coding region of the causative genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP557487.RAp_pph0jlvylOTIHMu_PJlUHIKruiRhNUYAb7hGRYJEU130_assertion description "[Spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2) and Machado-Joseph disease or spinocerebellar ataxia type 3 (MJD/SCA3) are three distinctive forms of autosomal dominant spinocerebellar ataxia (SCA) caused by expansions of an unstable CAG repeat localized in the coding region of the causative genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557487.RAp_pph0jlvylOTIHMu_PJlUHIKruiRhNUYAb7hGRYJEU130_provenance.
- NP1397484.RAvnBnwpt9MqBTNsyFAGCz84uksfQiswceTk3hg25fxL4130_assertion description "[Spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2) and Machado-Joseph disease or spinocerebellar ataxia type 3 (MJD/SCA3) are three distinctive forms of autosomal dominant spinocerebellar ataxia (SCA) caused by expansions of an unstable CAG repeat localized in the coding region of the causative genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1397484.RAvnBnwpt9MqBTNsyFAGCz84uksfQiswceTk3hg25fxL4130_provenance.