Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_provenance.
- NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_assertion description "[Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_provenance.
- NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_assertion evidence source_evidence_literature NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_provenance.
- NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_assertion SIO_000772 17292920 NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_provenance.
- NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_assertion wasDerivedFrom befree-20140225 NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_provenance.
- NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_assertion wasGeneratedBy ECO_0000203 NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP276166.RAqDNM5DHcbIfRtEwZJf7lf0-eqly44llhu2eMQC48GjI130_provenance.