Matches in Nanopublications for { ?s ?p "[Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant, late-onset neurodegenerative disease caused by a polyglutamine (polyQ) expansion in the ataxin-1 protein, which causes progressive neurodegeneration in cerebellar Purkinje cells and brainstem nuclei.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_assertion description "[Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant, late-onset neurodegenerative disease caused by a polyglutamine (polyQ) expansion in the ataxin-1 protein, which causes progressive neurodegeneration in cerebellar Purkinje cells and brainstem nuclei.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681593.RAS94yMFn6Ki9zkCrCoXjZtS7qjFreDnQInCS3At_CzgA130_provenance.
- NP1144625.RAMqya_Tcl5BxJ46qGq91ib8xcYOvfBrw8WqC1aES6YUc130_assertion description "[Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant, late-onset neurodegenerative disease caused by a polyglutamine (polyQ) expansion in the ataxin-1 protein, which causes progressive neurodegeneration in cerebellar Purkinje cells and brainstem nuclei.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1144625.RAMqya_Tcl5BxJ46qGq91ib8xcYOvfBrw8WqC1aES6YUc130_provenance.