Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_assertion> ?p ?o ?g. }
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- NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_assertion type Assertion NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_head.
- NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_assertion wasGeneratedBy ECO_0000203 NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_provenance.
- NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_assertion wasDerivedFrom befree-20150227 NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_provenance.
- NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_assertion SIO_000772 18418692 NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_provenance.
- NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_assertion evidence source_evidence_literature NP682021.RAq9jy0Z4QAryHEQu3jC0NdGJMojq736Jcey4GOSmYb6E130_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.