Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_provenance.
- NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_assertion description "[We analyzed 98 Japanese families with autosomal dominant SCAs, for whom CAG repeat expansions of the SCA1, SCA2, Machado-Joseph disease/SCA3, and dentatorubral-pallidoluysian atrophy genes were excluded, and 5 apparently sporadic cases of cortical cerebellar atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_provenance.
- NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_assertion evidence source_evidence_literature NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_provenance.
- NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_assertion SIO_000772 9403480 NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_provenance.
- NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_assertion wasDerivedFrom befree-20140225 NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_provenance.
- NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_assertion wasGeneratedBy ECO_0000203 NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_provenance.