Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_provenance.
- NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_assertion wasGeneratedBy ECO_0000203 NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_provenance.
- NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_assertion wasDerivedFrom befree-20150227 NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_provenance.
- NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_assertion SIO_000772 24816443 NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_provenance.
- NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_assertion evidence source_evidence_literature NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_provenance.
- NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_assertion description "[To date, a total of nine polyQ disorders have been described: six spinocerebellar ataxias (SCA) types 1, 2, 6, 7, 17; Machado-Joseph disease (MJD/SCA3); Huntington's disease (HD); dentatorubral pallidoluysian atrophy (DRPLA); and spinal and bulbar muscular atrophy, X-linked 1 (SMAX1/SBMA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251095.RAs2N4nvcUMTAvRbjG0qLOwZ9s-iSUzGYUQMRsPdZNRfU130_provenance.