Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_provenance.
- NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_assertion description "[Spinocerebellar ataxia type 6 (SCA6) was recently identified as a form of autosomal dominant cerebellar ataxia associated with small expansions of the trinucleotide repeat (CAG)n in the gene CACNL1A4 on chromosome 19p13, which encodes the alpha1 subunit of a P/Q-type voltage-gated calcium channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_provenance.
- NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_assertion evidence source_evidence_literature NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_provenance.
- NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_assertion SIO_000772 9403487 NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_provenance.
- NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_assertion wasDerivedFrom befree-20140225 NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_provenance.
- NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_assertion wasGeneratedBy ECO_0000203 NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP920227.RAUN_2B9ZYZZLjGcGeO99aIRaaZtZqhx6b2uOM2lpfOcA130_provenance.