Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_provenance.
- NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_assertion description "[Progression was faster in patients with SCA2 mutations and normal alleles with 22 or fewer repeats (P = .02) and in patients with SCA3 mutations with parkinsonism and/or dystonia at baseline (P = .003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_provenance.
- NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_assertion evidence source_evidence_literature NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_provenance.
- NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_assertion SIO_000772 22491195 NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_provenance.
- NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_assertion wasDerivedFrom befree-20150227 NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_provenance.
- NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_assertion wasGeneratedBy ECO_0000203 NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP541620.RAwuLEThua8fgJy2F8hx_68NBAqoBeZiYF4xaZlF4lvbo130_provenance.