Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_assertion> ?p ?o ?g. }
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- NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_assertion type Assertion NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_head.
- NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_assertion description "[Mucopolysaccharidosis type VI (MPS VI) is an autosomal recessive lysosomal storage disease caused by a deficiency of N-acetylgalactosamine-4-sulphatase (arylsulfatase B, ASB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_provenance.
- NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_assertion evidence source_evidence_literature NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_provenance.
- NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_assertion SIO_000772 11802522 NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_provenance.
- NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_assertion wasDerivedFrom befree-20150227 NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_provenance.
- NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_assertion wasGeneratedBy ECO_0000203 NP233218.RAG9kpituk6jj4OG9RMoXJzi5dDk-_4UPHbtNS4dQ_0_8130_provenance.