Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_assertion> ?p ?o ?g. }
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- NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_assertion type Assertion NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_head.
- NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_assertion wasGeneratedBy ECO_0000203 NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_provenance.
- NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_assertion wasDerivedFrom befree-2016 NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_provenance.
- NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_assertion SIO_000772 24849341 NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_provenance.
- NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_assertion evidence source_evidence_literature NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_provenance.
- NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_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." NP1184410.RA0dpRQQK8cLeaWBQfE2_Q9ijfn8ApQyGyac-M9xFSeno130_provenance.