Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_assertion> ?p ?o ?g. }
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- NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_assertion type Assertion NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_head.
- NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_assertion description "[Mucopolysaccharidosis type VI (MPS VI) or Maroteaux-Lamy syndrome, is a autosomal recessive disorder, due to the deficiency of the lysosomal enzyme N-acetylgalactosamine-4-sulfatase (arylsufatase B, ASB: EC 3.1.6.12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_provenance.
- NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_assertion evidence source_evidence_literature NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_provenance.
- NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_assertion SIO_000772 10206678 NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_provenance.
- NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_assertion wasDerivedFrom befree-20140225 NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_provenance.
- NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_assertion wasGeneratedBy ECO_0000203 NP568990.RA5mwbY6EqCL3urusR0CPYgCmofcb6Tw_5VsqGdVxYmU4130_provenance.