Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_assertion> ?p ?o ?g. }
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- NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_assertion type Assertion NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_head.
- NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_assertion wasGeneratedBy ECO_0000203 NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_provenance.
- NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_assertion wasDerivedFrom befree-20150227 NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_provenance.
- NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_assertion SIO_000772 23030542 NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_provenance.
- NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_assertion evidence source_evidence_literature NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_provenance.
- NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_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." NP277106.RAWtBCk96FnY-SY3cvX95lRhEZPqUualJSAu_RLuWhlhw130_provenance.