Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_provenance.
- 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.
- uniprot-20150221 importedOn "2015-02-21" NP1718.RAmKHTnLof-kQE4tnLbbpR1FDyN_6vqDpu9wNKupfu2vI130_provenance.