Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_provenance.
- NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_assertion description "[Compilation of the clinical records of 43 patients with documented mutation in the alpha-TTP gene revealed differences from Friedreich ataxia: cardiomyopathy was found in only 19% of cases, whereas head titubation was found in 28% of cases and dystonia in an additional 13%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_provenance.
- NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_assertion evidence source_evidence_literature NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_provenance.
- NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_assertion SIO_000772 9463307 NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_provenance.
- NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_assertion wasDerivedFrom befree-20140225 NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_provenance.
- NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_assertion wasGeneratedBy ECO_0000203 NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP586044.RAt5zp6dDwm5w96_grFLO0jUq01QfD1UjPDwvm7ctW31I130_provenance.