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- source_evidence_literature type ECO_0000212 NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP333902.RAfSvswL-5F9DTJY38JOuYwOWDqUd4OTpemIMD1KuomgM130_provenance.