Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_assertion> ?p ?o ?g. }
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- NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_assertion type Assertion NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_head.
- NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_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." NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_provenance.
- NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_assertion evidence source_evidence_curated NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_provenance.
- NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_assertion SIO_000772 10206678 NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_provenance.
- NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_assertion wasDerivedFrom uniprot-20130724 NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_provenance.
- NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_assertion wasGeneratedBy ECO_0000218 NP507.RATm2QxFxVByywFwTxeFgH4ExCi4vbjsyv_NbDubyGXlk130_provenance.