Full identifier: https://w3id.org/kpxl/ios/ds/np/RA_16AtkD9jTpytHbpHYkGM8DK1kUORRi_GjyRuznydI0#spi
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NGLY1 deficiency is a novel autosomal recessive disorder of the ERAD pathway. DataScience SuperPatternInstance ▼ comment approve/disapprove edit as derived nanopublication create new with same template
Núria Queralt Rosinach (author), Tobias Kuhn (creator), 9 Apr 2025, 06:33:41 UTC
TriG(txt), JSON-LD(txt), N-Quads(txt), XML(txt)