Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_assertion> ?p ?o ?g. }
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- NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_assertion type Assertion NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_head.
- NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_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." NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_provenance.
- NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_assertion evidence source_evidence_curated NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_provenance.
- NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_assertion SIO_000772 10206678 NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_provenance.
- NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_assertion wasDerivedFrom uniprot-20150221 NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_provenance.
- NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_assertion wasGeneratedBy ECO_0000218 NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_provenance.