Matches in Nanopublications for { ?s ?p "[Spinocerebellar ataxia 36 (SCA36) is an autosomal-dominant neurodegenerative disorder caused by a large (>650) hexanucleotide GGCCTG repeat expansion in the first intron of the NOP56 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 4 of
4
with 100 items per page.
- assertion description "[Spinocerebellar ataxia 36 (SCA36) is an autosomal-dominant neurodegenerative disorder caused by a large (>650) hexanucleotide GGCCTG repeat expansion in the first intron of the NOP56 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Spinocerebellar ataxia 36 (SCA36) is an autosomal-dominant neurodegenerative disorder caused by a large (>650) hexanucleotide GGCCTG repeat expansion in the first intron of the NOP56 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_assertion description "[Spinocerebellar ataxia 36 (SCA36) is an autosomal-dominant neurodegenerative disorder caused by a large (>650) hexanucleotide GGCCTG repeat expansion in the first intron of the NOP56 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_provenance.
- NP1244905.RA2_Mpzvpp7HhAvp6vVo6aHI5LrTZTg2BAr_iPckaObMU130_assertion description "[Spinocerebellar ataxia 36 (SCA36) is an autosomal-dominant neurodegenerative disorder caused by a large (>650) hexanucleotide GGCCTG repeat expansion in the first intron of the NOP56 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244905.RA2_Mpzvpp7HhAvp6vVo6aHI5LrTZTg2BAr_iPckaObMU130_provenance.