Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_provenance.
- NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_assertion wasGeneratedBy ECO_0000203 NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_provenance.
- NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_assertion wasDerivedFrom befree-2016 NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_provenance.
- NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_assertion SIO_000772 24092288 NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_provenance.
- NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_assertion evidence source_evidence_literature NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_provenance.
- NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_assertion description "[Combined dystonias (with parkinsonism or myoclonus) are further subdivided into persistent (GCHI [DYT5], SGCE [DYT11], and ATP1A3 [DYT12], with TAF1 most likely but not yet proven to be linked to DYT3) and paroxysmal (PNKD [DYT8], PRRT2 [DYT10], and SLC2A1 [DYT18]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116046.RApBcWTznacoTr1ggFgN2Mvw20isyi91u1SGeOEqM4Th4130_provenance.