Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_provenance.
- NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_assertion description "[We determined the prevalence of SCA2 and SCA3 mutations in a cohort of ET and atypical Parkinsonism patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_provenance.
- NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_assertion evidence source_evidence_literature NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_provenance.
- NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_assertion SIO_000772 17712857 NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_provenance.
- NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_assertion wasDerivedFrom lhgdn-20090331 NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_provenance.
- NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_assertion wasGeneratedBy ECO_0000203 NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_provenance.