Matches in Nanopublications for { ?s ?p "[Spinocerebellar ataxia type 17 (SCA17) is an autosomal dominant cerebellar ataxia caused by expansion of CAG/CAA trinucleotide repeats in the TATA-binding protein (TBP) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP373971.RAA5t4WBVlYi1XERDfD0kKjra3c03mlC-6MvWIaB_AoUo130_assertion description "[Spinocerebellar ataxia type 17 (SCA17) is an autosomal dominant cerebellar ataxia caused by expansion of CAG/CAA trinucleotide repeats in the TATA-binding protein (TBP) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373971.RAA5t4WBVlYi1XERDfD0kKjra3c03mlC-6MvWIaB_AoUo130_provenance.
- NP723857.RAAlt2N5NU4Vmy4914z_B-QlPgFEw62X7hq2L9n7-5oVE130_assertion description "[Spinocerebellar ataxia type 17 (SCA17) is an autosomal dominant cerebellar ataxia caused by expansion of CAG/CAA trinucleotide repeats in the TATA-binding protein (TBP) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723857.RAAlt2N5NU4Vmy4914z_B-QlPgFEw62X7hq2L9n7-5oVE130_provenance.
- NP593891.RAKvMP2vCvIbhpkJShzIBFzD7au5ZpjsKRNtI1H6Ej4zc130_assertion description "[Spinocerebellar ataxia type 17 (SCA17) is an autosomal dominant cerebellar ataxia caused by expansion of CAG/CAA trinucleotide repeats in the TATA-binding protein (TBP) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593891.RAKvMP2vCvIbhpkJShzIBFzD7au5ZpjsKRNtI1H6Ej4zc130_provenance.
- NP431992.RACt9SQvSeLY9sxEUc0UJJOhIi-LgSYG_8pDKeQ28jxlw130_assertion description "[Spinocerebellar ataxia type 17 (SCA17) is an autosomal dominant cerebellar ataxia caused by expansion of CAG/CAA trinucleotide repeats in the TATA-binding protein (TBP) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431992.RACt9SQvSeLY9sxEUc0UJJOhIi-LgSYG_8pDKeQ28jxlw130_provenance.
- assertion description "[Spinocerebellar ataxia type 17 (SCA17) is an autosomal dominant cerebellar ataxia caused by expansion of CAG/CAA trinucleotide repeats in the TATA-binding protein (TBP) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Spinocerebellar ataxia type 17 (SCA17) is an autosomal dominant cerebellar ataxia caused by expansion of CAG/CAA trinucleotide repeats in the TATA-binding protein (TBP) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_assertion description "[Spinocerebellar ataxia type 17 (SCA17) is an autosomal dominant cerebellar ataxia caused by expansion of CAG/CAA trinucleotide repeats in the TATA-binding protein (TBP) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_provenance.