Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_provenance.
- NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_assertion description "[Spinocerebellar ataxia type 6 (SCA6) is an inherited neurodegenerative disease caused by a polyglutamine (polyQ) expansion in the Ca(V)2.1 voltage-gated calcium channel subunit (CACNA1A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_provenance.
- NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_assertion evidence source_evidence_literature NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_provenance.
- NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_assertion SIO_000772 21550405 NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_provenance.
- NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_assertion wasDerivedFrom befree-20140225 NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_provenance.
- NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_assertion wasGeneratedBy ECO_0000203 NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP900368.RA5wgWi_li5ONDdRjhd1hnXMM5dBRHdKXiXtXKEP5Q-2U130_provenance.