Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_provenance.
- NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_assertion description "[However, at least half of dominant ataxias (SCAs) are caused by (CAG)n repeat expansions resulting in expanded polyglutamine tracts (SCAs 1, 2, 3, 6, 7, 17, and DRPLA), although of the remainder only SCAs 8, 10, 12, 14, 15/16, and 31 are frequent enough that the described phenotype is probably representative.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_provenance.
- NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_assertion evidence source_evidence_literature NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_provenance.
- NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_assertion SIO_000772 25192506 NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_provenance.
- NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_assertion wasDerivedFrom befree-2016 NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_provenance.
- NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_assertion wasGeneratedBy ECO_0000203 NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1217269.RAbYivp8IesWOZnG3Bh0CD4e0xhq4abO9hoK_8eIUMOnY130_provenance.