Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_provenance.
- NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_assertion description "[Machado-Joseph disease (spinocerebellar ataxia type 3) (prevalence, 3.1 per 100,000 population), Friedreich ataxia (prevalence, 1.0 per 100,000 population), and ataxia with oculomotor apraxia (prevalence, 0.4 per 100,000 population) were the most frequent HCAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_provenance.
- NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_assertion evidence source_evidence_literature NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_provenance.
- NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_assertion SIO_000772 23609960 NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_provenance.
- NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_assertion wasDerivedFrom befree-20150227 NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_provenance.
- NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_assertion wasGeneratedBy ECO_0000203 NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP411520.RAFEmwcZ1iXzwbHPLs3HJe3KC2tmr7ypPmQPxr-FVl60M130_provenance.