Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_assertion> ?p ?o ?g. }
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- NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_assertion type Assertion NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_head.
- 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.
- NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_assertion evidence source_evidence_literature NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_provenance.
- NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_assertion SIO_000772 25476002 NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_provenance.
- NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_assertion wasDerivedFrom befree-2016 NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_provenance.
- NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_assertion wasGeneratedBy ECO_0000203 NP1244906.RAsVlUu1fopyKPYz7fc7StCDjVIS5tYkKkJ4HYYDgTnpA130_provenance.