Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_provenance.
- NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_assertion wasGeneratedBy ECO_0000203 NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_provenance.
- NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_assertion wasDerivedFrom befree-20140225 NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_provenance.
- NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_assertion SIO_000772 18418692 NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_provenance.
- NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_assertion evidence source_evidence_literature NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_provenance.
- NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_assertion description "[Spinocerebellar ataxia type 8 (SCA8) is a dominantly inherited, slowly progressive neurodegenerative disorder caused by a CTG.CAG repeat expansion located on chromosome 13q21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP798359.RAyfyEqc8xEq6bxClIzGA8YEnnigU6cxYB1Wo6FyhvcPY130_provenance.