Matches in Nanopublications for { ?s ?p "[Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP248383.RASkPLc-G2vbfJLrPexXC_rT5gVF0DnSsu357FHqpcvjU130_assertion description "[Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248383.RASkPLc-G2vbfJLrPexXC_rT5gVF0DnSsu357FHqpcvjU130_provenance.
- NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_assertion description "[Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_provenance.
- NP923880.RA69rO5lmh4FsEj3sLNJjqTbHy6HVL3QGaCUfsGZpQoGU130_assertion description "[Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923880.RA69rO5lmh4FsEj3sLNJjqTbHy6HVL3QGaCUfsGZpQoGU130_provenance.
- NP666477.RA1ofxpy7LTndGm7g-J6v-qooKQc24sRFRvjJYjUTemC8130_assertion description "[Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666477.RA1ofxpy7LTndGm7g-J6v-qooKQc24sRFRvjJYjUTemC8130_provenance.
- NP681993.RAIYy4_JA4A5cgDS5GibFnJ_Ai3jsmyHhDWoUcuMAnmeA130_assertion description "[Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681993.RAIYy4_JA4A5cgDS5GibFnJ_Ai3jsmyHhDWoUcuMAnmeA130_provenance.
- NP923829.RAOo5cBEiEGnzjXqvO9eh3XOwgPVA4HyWdvLpt-7G2P-8130_assertion description "[Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923829.RAOo5cBEiEGnzjXqvO9eh3XOwgPVA4HyWdvLpt-7G2P-8130_provenance.
- NP666474.RAPlVFbOKYAh2Drfj8-0sDk9vRjzqj2QbgnDR4AGmGuG0130_assertion description "[Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666474.RAPlVFbOKYAh2Drfj8-0sDk9vRjzqj2QbgnDR4AGmGuG0130_provenance.
- NP666478.RAOdCy_UbcLoNXgNHCHvX1exmcE_6bF8RTm25npEg7HFs130_assertion description "[Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666478.RAOdCy_UbcLoNXgNHCHvX1exmcE_6bF8RTm25npEg7HFs130_provenance.
- NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_assertion description "[Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_provenance.
- NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_assertion description "[Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_provenance.