Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_provenance.
- NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_assertion wasGeneratedBy ECO_0000203 NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_provenance.
- NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_assertion wasDerivedFrom befree-2016 NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_provenance.
- NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_assertion SIO_000772 25131594 NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_provenance.
- NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_assertion evidence source_evidence_literature NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_provenance.
- NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_assertion description "[PolyQ (polyglutamine) diseases such as HD (Huntington's disease) or SCA1 (spinocerebellar ataxia type 1) are neurodegenerative disorders caused by abnormally elongated polyQ tracts in human proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211452.RA8h8lD7ktrcy7RRecGa8vCdUCA1kkeLuBfW08iUhNVwA130_provenance.