Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_assertion type Assertion NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_head.
- NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_assertion description "[Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are responsible for a severe neurological disorder known as Unverricht-Lundborg disease (EPM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_provenance.
- NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_assertion evidence source_evidence_literature NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_provenance.
- NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_assertion SIO_000772 9806543 NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_provenance.
- NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_assertion wasDerivedFrom befree-20150227 NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_provenance.
- NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_assertion wasGeneratedBy ECO_0000203 NP337244.RA2w6KLXlMtWbcLefbqtS-E-3BfggLZZjtSRz98skEUQs130_provenance.