Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_provenance.
- NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_assertion description "[Among the 15 sporadic SCA patients, genetic mutations for SCA2, SCA6, SCA17, and SCA31 were identified, indicating that ADCAs should be considered in sporadic cases of ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_provenance.
- NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_assertion evidence source_evidence_literature NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_provenance.
- NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_assertion SIO_000772 21088341 NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_provenance.
- NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_assertion wasDerivedFrom befree-20140225 NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_provenance.
- NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_assertion wasGeneratedBy ECO_0000203 NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP176610.RAUn8zMDS9Yop-GkQXTHzCZdGaH1lo92YsomnE-IwySmc130_provenance.