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- NP810567.RASQCJ-dVnrH6VyJrt8ZzxvTGDNpOeeUqjXGWewZV0V7c130_assertion type Assertion NP810567.RASQCJ-dVnrH6VyJrt8ZzxvTGDNpOeeUqjXGWewZV0V7c130_head.
- NP810567.RASQCJ-dVnrH6VyJrt8ZzxvTGDNpOeeUqjXGWewZV0V7c130_assertion wasGeneratedBy ECO_0000203 NP810567.RASQCJ-dVnrH6VyJrt8ZzxvTGDNpOeeUqjXGWewZV0V7c130_provenance.
- NP810567.RASQCJ-dVnrH6VyJrt8ZzxvTGDNpOeeUqjXGWewZV0V7c130_assertion wasDerivedFrom befree-20140225 NP810567.RASQCJ-dVnrH6VyJrt8ZzxvTGDNpOeeUqjXGWewZV0V7c130_provenance.
- NP810567.RASQCJ-dVnrH6VyJrt8ZzxvTGDNpOeeUqjXGWewZV0V7c130_assertion SIO_000772 19479962 NP810567.RASQCJ-dVnrH6VyJrt8ZzxvTGDNpOeeUqjXGWewZV0V7c130_provenance.
- NP810567.RASQCJ-dVnrH6VyJrt8ZzxvTGDNpOeeUqjXGWewZV0V7c130_assertion evidence source_evidence_literature NP810567.RASQCJ-dVnrH6VyJrt8ZzxvTGDNpOeeUqjXGWewZV0V7c130_provenance.
- NP810567.RASQCJ-dVnrH6VyJrt8ZzxvTGDNpOeeUqjXGWewZV0V7c130_assertion description "[Mucopolysaccharidosis (MPS) type IIIC or Sanfilippo syndrome type C is a rare autosomal recessive disorder caused by the deficiency of the lysosomal membrane enzyme, heparan sulfate acetyl-CoA (AcCoA): alpha-glucosaminide N-acetyltransferase (HGSNAT; EC 2.3.1.78), which catalyzes transmembrane acetylation of the terminal glucosamine residues of heparan sulfate prior to their hydrolysis by alpha-N-acetylglucosaminidase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810567.RASQCJ-dVnrH6VyJrt8ZzxvTGDNpOeeUqjXGWewZV0V7c130_provenance.