Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_assertion> ?p ?o ?g. }
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- NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_assertion type Assertion NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_head.
- NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_assertion description "[Hunter disease (mucopolysaccharidosis type II or MPS II) is an X-linked recessive disorder caused by the deficiency of the lysosomal enzyme iduronate-2-sulfatase (IDS) (E.C.3.1.6.13.) involved in the catabolism of mucopolysaccharides dermatan sulfate and heparan sulfate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_provenance.
- NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_assertion evidence source_evidence_curated NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_provenance.
- NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_assertion SIO_000772 10215411 NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_provenance.
- NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_assertion wasDerivedFrom uniprot-2016 NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_provenance.
- NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_assertion wasGeneratedBy ECO_0000218 NP132.RAQXJRvXJdSsbxjZw9lOrIsXKYIGami7eVBDVurKPbq8c130_provenance.