Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance.
- NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_assertion description "[Machado-Joseph disease (MJD), one of the most common types of hereditary spinocerebellar degeneration caused by abnormal expansion of the CAG repeat in the MJD1 gene, presents atrophy of the infratentorial structures neuropathologically and neuroradiologically.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance.
- NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_assertion evidence source_evidence_literature NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance.
- NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_assertion SIO_000772 18042234 NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance.
- NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_assertion wasDerivedFrom befree-20140225 NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance.
- NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_assertion wasGeneratedBy ECO_0000203 NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance.