Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_provenance.
- NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_assertion description "[Spinocerebellar ataxia type 15 (SCA15) is an autosomal dominant neurodegenerative disorder clinically characterized by late-onset, slowly progressive pure cerebellar ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_provenance.
- NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_assertion evidence source_evidence_literature NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_provenance.
- NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_assertion SIO_000772 22318346 NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_provenance.
- NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_assertion wasDerivedFrom befree-20140225 NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_provenance.
- NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_assertion wasGeneratedBy ECO_0000203 NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP723973.RAeDZSMdupcM_3vmS9ijCUDTpBGT7OmecfrNk2kcAHfE0130_provenance.