Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_provenance.
- befree-2016 importedOn "2016-02-19" NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_provenance.
- NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_assertion wasGeneratedBy ECO_0000203 NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_provenance.
- NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_assertion wasDerivedFrom befree-2016 NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_provenance.
- NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_assertion SIO_000772 17440947 NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_provenance.
- NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_assertion evidence source_evidence_literature NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_provenance.
- NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_assertion description "[Recent reports suggest that CAG triplet expansions of spinocerebellar ataxia type 2 and 3 (SCA2 and SCA3) genes are the cause of typical levodopa-responsive Parkinson's disease (PD) in familial cases, several of which were ethnic Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605201.RABt97qHjxcr4blM7GY8EyP9D1dghMC5-f5UtFxGe6kK0130_provenance.