Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_assertion> ?p ?o ?g. }
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- NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_assertion type Assertion NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_head.
- NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_assertion description "[Metachromatic leukodystrophy (MLD) is an autosomal recessive storage disease caused by deficiency of the lysosomal enzyme, arylsulfatase A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_provenance.
- NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_assertion evidence source_evidence_curated NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_provenance.
- NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_assertion SIO_000772 9600244 NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_provenance.
- NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_assertion wasDerivedFrom uniprot-2016 NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_provenance.
- NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_assertion wasGeneratedBy ECO_0000218 NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_provenance.