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- NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_assertion type Assertion NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_head.
- NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_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." NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_provenance.
- NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_assertion evidence source_evidence_literature NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_provenance.
- NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_assertion SIO_000772 17292920 NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_provenance.
- NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_assertion wasDerivedFrom befree-20140225 NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_provenance.
- NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_assertion wasGeneratedBy ECO_0000203 NP812863.RAnHUZHJjsU1_f_4QyPzcZL2kcrUgM4EMYlFrl4BNUTpk130_provenance.