Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_assertion> ?p ?o ?g. }
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- NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_assertion type Assertion NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_head.
- NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_assertion wasGeneratedBy ECO_0000203 NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_provenance.
- NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_assertion wasDerivedFrom befree-20150227 NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_provenance.
- NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_assertion SIO_000772 24849341 NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_provenance.
- NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_assertion evidence source_evidence_literature NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_provenance.
- NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_assertion description "[Specific missense mutations in the CACNA1A gene, which encodes a subunit of voltage-gated CaV2.1 channels, are associated with familial hemiplegic migraine type 1 (FHM1), a rare monogenic subtype of common migraine with aura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_provenance.