Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_assertion> ?p ?o ?g. }
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- NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_assertion type Assertion NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_head.
- NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_assertion description "[The clinical features of these patients were late onset progressive pure cerebellar ataxia with dysarthria and nystagmus, and are consistent with autosomal dominant cerebellar ataxia type III (ADCA type III).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_provenance.
- NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_assertion evidence source_evidence_literature NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_provenance.
- NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_assertion SIO_000772 9600677 NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_provenance.
- NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_assertion wasDerivedFrom befree-20150227 NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_provenance.
- NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_assertion wasGeneratedBy ECO_0000203 NP615049.RAii7tWzQg8u96XQYwaQh1lx0RyZg1zxjELN8P7K9Wczs130_provenance.