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- NP671318.RA_-J5w6YhvITsM6-V5uP69N5zrCkwP6BepPEtFE_nZv0130_assertion type Assertion NP671318.RA_-J5w6YhvITsM6-V5uP69N5zrCkwP6BepPEtFE_nZv0130_head.
- NP671318.RA_-J5w6YhvITsM6-V5uP69N5zrCkwP6BepPEtFE_nZv0130_assertion wasGeneratedBy ECO_0000203 NP671318.RA_-J5w6YhvITsM6-V5uP69N5zrCkwP6BepPEtFE_nZv0130_provenance.
- NP671318.RA_-J5w6YhvITsM6-V5uP69N5zrCkwP6BepPEtFE_nZv0130_assertion wasDerivedFrom befree-20140225 NP671318.RA_-J5w6YhvITsM6-V5uP69N5zrCkwP6BepPEtFE_nZv0130_provenance.
- NP671318.RA_-J5w6YhvITsM6-V5uP69N5zrCkwP6BepPEtFE_nZv0130_assertion SIO_000772 23030542 NP671318.RA_-J5w6YhvITsM6-V5uP69N5zrCkwP6BepPEtFE_nZv0130_provenance.
- NP671318.RA_-J5w6YhvITsM6-V5uP69N5zrCkwP6BepPEtFE_nZv0130_assertion evidence source_evidence_literature NP671318.RA_-J5w6YhvITsM6-V5uP69N5zrCkwP6BepPEtFE_nZv0130_provenance.
- NP671318.RA_-J5w6YhvITsM6-V5uP69N5zrCkwP6BepPEtFE_nZv0130_assertion description "[Genetic studies in the rare form of familial hemiplegic migraine have identified mutations in 3 genes (CACNA1A, ATP1A2, and SCN1A) encoding proteins involved in ion homeostasis and suggesting that other such genes may be involved in the more common forms of migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671318.RA_-J5w6YhvITsM6-V5uP69N5zrCkwP6BepPEtFE_nZv0130_provenance.