Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_assertion> ?p ?o ?g. }
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- NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_assertion type Assertion NP111006.RAoYs_AMpaS6eNoQjnVCsgVrq3PgDVTxdL4Q8rdwIlmno130_head.
- 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.