Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_assertion type Assertion NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_head.
- NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_provenance.
- NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_assertion evidence source_evidence_literature NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_provenance.
- NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_assertion SIO_000772 17292920 NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_provenance.
- NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_assertion wasDerivedFrom befree-2016 NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_provenance.
- NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_assertion wasGeneratedBy ECO_0000203 NP593268.RADpTObMHLbn0KtegKQYlQGO6Ejitjb17VqadO4oEitew130_provenance.