Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_assertion type Assertion NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_head.
- NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_assertion description "[Unverricht-Lundborg disease (ULD), progressive myoclonic epilepsy type 1 (EPM1, OMIM254800), is an autosomal recessively inherited neurodegenerative disorder characterized by age of onset from 6 to 16 years, stimulus-sensitive myoclonus, and tonic-clonic epileptic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.
- NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_assertion evidence source_evidence_literature NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.
- NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_assertion SIO_000772 18325013 NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.
- NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_assertion wasDerivedFrom befree-20150227 NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.
- NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_assertion wasGeneratedBy ECO_0000203 NP333851.RAC9LauUsnbg7B0azTR8IKgTOtxvRAI1g9sVwS6yd5p4o130_provenance.