Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP277068.RAfp9zkQyi1iIbLcVH5MuUuHnrHby8_Xvc25H7VK1azzw130_provenance.
- 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.