Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_assertion type Assertion NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_head.
- NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_assertion description "[Progressive myoclonus epilepsy 1 (EPM1) or Unverricht-Lundborg disease is a human autosomal recessive neurodegenerative disorder caused by mutations in cystatin B (CSTB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_provenance.
- NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_assertion evidence source_evidence_literature NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_provenance.
- NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_assertion SIO_000772 14526183 NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_provenance.
- NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_assertion wasDerivedFrom befree-20150227 NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_provenance.
- NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_assertion wasGeneratedBy ECO_0000203 NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_provenance.