Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_provenance.
- NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_assertion description "[Spinocerebellar ataxia type 6 (SCA6) was recently identified as a form of autosomal dominant spinocerebellar ataxia associated with a small CAG repeat expansion of the gene encoding an alpha 1 A-voltage-dependent calcium channel gene subunit on chromosome 19p13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_provenance.
- NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_assertion evidence source_evidence_literature NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_provenance.
- NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_assertion SIO_000772 10985694 NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_provenance.
- NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_assertion wasDerivedFrom befree-20150227 NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_provenance.
- NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_assertion wasGeneratedBy ECO_0000203 NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP226059.RAIRnVev8FufwO77X88oVJQekmWfYA9o8KYt9hax-Iar8130_provenance.