Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_assertion> ?p ?o ?g. }
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- NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_assertion type Assertion NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_head.
- NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_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." NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_provenance.
- NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_assertion evidence source_evidence_literature NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_provenance.
- NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_assertion SIO_000772 14526183 NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_provenance.
- NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_assertion wasDerivedFrom befree-20140225 NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_provenance.
- NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_assertion wasGeneratedBy ECO_0000203 NP181677.RA78RcfCfu97nQgAQhLnzV1Zdj2hEt4rLDQeHmnDlZPtY130_provenance.