Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_assertion> ?p ?o ?g. }
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- NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_assertion type Assertion NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_head.
- 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.
- NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_assertion evidence source_evidence_curated NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_provenance.
- NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_assertion SIO_000772 11802522 NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_provenance.
- NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_assertion wasDerivedFrom uniprot-2016 NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_provenance.
- NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_assertion wasGeneratedBy ECO_0000218 NP1831.RAB9F8E8iUUJAx8heDqRIxZVgInjbpwuFVZiKbghmx3_Q130_provenance.