Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_provenance.
- NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_assertion description "[We compared horizontal eye movements (visually guided saccades, antisaccades, and smooth pursuit) in control subjects (n = 14) and patients with three forms of autosomal dominant cerebellar ataxias type I: spinocerebellar ataxias 1 and 2 (SCA1, n = 11; SCA2, n = 10) and SCA3/Machado-Joseph disease (MJD) (n = 16).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_provenance.
- NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_assertion evidence source_evidence_literature NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_provenance.
- NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_assertion SIO_000772 9506545 NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_provenance.
- NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_assertion wasDerivedFrom befree-20140225 NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_provenance.
- NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_assertion wasGeneratedBy ECO_0000203 NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_provenance.
- befree-20140225 importedOn "2014-02-25" NP487398.RAj1KqqrK8WL0TV_LW9vGE4PEOOetS4iPYOElevZ_X2Ok130_provenance.