Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_assertion> ?p ?o ?g. }
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- NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_assertion type Assertion NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_head.
- NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_assertion wasGeneratedBy ECO_0000203 NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_provenance.
- NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_assertion wasDerivedFrom befree-2016 NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_provenance.
- NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_assertion SIO_000772 18418692 NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_provenance.
- NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_assertion evidence source_evidence_literature NP666473.RAuApZmCGj36YkcNnn6E8MBeYsS1s03DQtvfmAtd-TerU130_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.