Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_provenance.
- NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_assertion description "[Mutation analyses for SCA1, 2, 3, 6, 7, 8, 10, 12, 17, and DRPLA and frataxin genes were performed for 251 unrelated Finnish patients who presented with progressive ataxia disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_provenance.
- NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_assertion evidence source_evidence_literature NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_provenance.
- NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_assertion SIO_000772 15691283 NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_provenance.
- NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_assertion wasDerivedFrom befree-20140225 NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_provenance.
- NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_assertion wasGeneratedBy ECO_0000203 NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP605084.RA4s5njCPksxdD2DBnSpOGXaG9brqFmUFo2kcjRWhA79s130_provenance.