Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_provenance.
- NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_assertion description "[We found that SCA3/MJD was the most common type of autosomal dominant SCA in Mainland Chinese, accounting for 83 patients from 59 families (49.2%), followed by SCA2 (8 [6.7%]), SCA1 (7 [5.8%]), SCA6 (4 [3.3%]), SCA7 (1 [0.8%]), SCA8 (0%), SCA10 (0%), SCA12 (1 [0.8%]), SCA14 (0%), SCA17 (0%) and DRPLA (0%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_provenance.
- NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_assertion evidence source_evidence_literature NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_provenance.
- NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_assertion SIO_000772 15979648 NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_provenance.
- NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_assertion wasDerivedFrom befree-20140225 NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_provenance.
- NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_assertion wasGeneratedBy ECO_0000203 NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_provenance.
- befree-20140225 importedOn "2014-02-25" NP179717.RAVjPXe79XF3MgnxBcgH4SlOronbPEqvo0-MRxWg3n8ys130_provenance.