Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_provenance.
- NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_assertion description "[Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_provenance.
- NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_assertion evidence source_evidence_literature NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_provenance.
- NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_assertion SIO_000772 19182766 NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_provenance.
- NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_assertion wasDerivedFrom befree-2016 NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_provenance.
- NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_assertion wasGeneratedBy ECO_0000203 NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_provenance.
- befree-2016 importedOn "2016-02-19" NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_provenance.