Full identifier: http://purl.org/np/RASPvPrnUq6SOsOkrgOsUvRbsfmC7dHd73FgUA6oRmlGg#assertion
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NGLY1 deficiency is a novel autosomal recessive disorder of the ERAD pathway. SuperPatternInstance ▼ comment approve/disapprove edit as derived nanopublication create new with same template
Núria Queralt Rosinach, 8 Dec 2021, 15:48:24 UTC
TriG(txt), JSON-LD(txt), N-Quads(txt), XML(txt)