Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_provenance.
- NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_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." NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_provenance.
- NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_assertion evidence source_evidence_literature NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_provenance.
- NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_assertion SIO_000772 9506545 NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_provenance.
- NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_assertion wasDerivedFrom befree-2016 NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_provenance.
- NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_assertion wasGeneratedBy ECO_0000203 NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1390777.RAiV_t92XrTozHpz4hH1LtbVewk-CJHMWEGI2jkcoGacQ130_provenance.