Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_assertion> ?p ?o ?g. }
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- NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_assertion type Assertion NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_head.
- NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_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." NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_provenance.
- NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_assertion evidence source_evidence_literature NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_provenance.
- NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_assertion SIO_000772 17292920 NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_provenance.
- NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_assertion wasDerivedFrom befree-20140225 NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_provenance.
- NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_assertion wasGeneratedBy ECO_0000203 NP520055.RAAVPIYoQxYIoJKF-LREywAT4BiJv7HoAocqWwz5U4omA130_provenance.