Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP511.RAUOxzOhVIr2xvuliGPLEu2iwKv_IkmAYieM81T_Br1eM130_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." NP511.RAUOxzOhVIr2xvuliGPLEu2iwKv_IkmAYieM81T_Br1eM130_provenance.
- 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." provenance.
- 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." provenance.
- NP709673.RAtAMFE31rNCcs9ge-PAqhkfGkiKmG83nJTA2yc_7Alco130_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." NP709673.RAtAMFE31rNCcs9ge-PAqhkfGkiKmG83nJTA2yc_7Alco130_provenance.
- NP1722.RAj3IJL_qqS9iwGRbMPMKrVWmdySnETE_nN7QIzhChuBw130_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." NP1722.RAj3IJL_qqS9iwGRbMPMKrVWmdySnETE_nN7QIzhChuBw130_provenance.
- NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_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." NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_provenance.
- NP342579.RAp3wYBcySCFDpB629jQBlsbNozzyEkm2-ie3abJYYx5c130_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." NP342579.RAp3wYBcySCFDpB629jQBlsbNozzyEkm2-ie3abJYYx5c130_provenance.
- 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.
- NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_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." NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_provenance.