Matches in Nanopublications for { ?s ?p "[Huntington's disease (HD), spinocerebellar ataxias types 1 and 3 (SCA1, SCA3), and spinobulbar muscular atrophy (SBMA) are caused by CAG/polyglutamine expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP600890.RARfxVaLOidKTSUrLuKJu2hxXIrOMMVZAHzntzJhNBmdc130_assertion description "[Huntington's disease (HD), spinocerebellar ataxias types 1 and 3 (SCA1, SCA3), and spinobulbar muscular atrophy (SBMA) are caused by CAG/polyglutamine expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600890.RARfxVaLOidKTSUrLuKJu2hxXIrOMMVZAHzntzJhNBmdc130_provenance.
- NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_assertion description "[Huntington's disease (HD), spinocerebellar ataxias types 1 and 3 (SCA1, SCA3), and spinobulbar muscular atrophy (SBMA) are caused by CAG/polyglutamine expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_provenance.
- NP428655.RAIaMGsZbplRG8351Y3bBu1hGWMWCB5WjHyjdnKpwh_ik130_assertion description "[Huntington's disease (HD), spinocerebellar ataxias types 1 and 3 (SCA1, SCA3), and spinobulbar muscular atrophy (SBMA) are caused by CAG/polyglutamine expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428655.RAIaMGsZbplRG8351Y3bBu1hGWMWCB5WjHyjdnKpwh_ik130_provenance.
- assertion description "[Huntington's disease (HD), spinocerebellar ataxias types 1 and 3 (SCA1, SCA3), and spinobulbar muscular atrophy (SBMA) are caused by CAG/polyglutamine expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Huntington's disease (HD), spinocerebellar ataxias types 1 and 3 (SCA1, SCA3), and spinobulbar muscular atrophy (SBMA) are caused by CAG/polyglutamine expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Huntington's disease (HD), spinocerebellar ataxias types 1 and 3 (SCA1, SCA3), and spinobulbar muscular atrophy (SBMA) are caused by CAG/polyglutamine expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.