Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_assertion type Assertion NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_head.
- NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_assertion description "[Episodic ataxia type 1 (EA1) is caused by mutations in the KCNA1 gene encoding the fast potassium channel Kv1.1 and is characterized clinically by brief episodes of ataxia and continuous and spontaneous motor unit activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.
- NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_assertion evidence source_evidence_literature NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.
- NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_assertion SIO_000772 23909822 NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.
- NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_assertion wasDerivedFrom befree-20150227 NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.
- NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_assertion wasGeneratedBy ECO_0000203 NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.