Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_provenance.
- NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_assertion description "[Spinocerebellar ataxia type 31 (SCA31), is a recently defined subtype of autosomal dominant cerebellar ataxia (ADCA) characterized by late-onset pure cerebellar ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_provenance.
- NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_assertion evidence source_evidence_literature NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_provenance.
- NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_assertion SIO_000772 22353852 NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_provenance.
- NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_assertion wasDerivedFrom befree-20150227 NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_provenance.
- NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_assertion wasGeneratedBy ECO_0000203 NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP974682.RAfiNq-ptPCDd1JnBxSE1FVQNG9Y5oDE2LsKPS00IZfTg130_provenance.