Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_provenance.
- 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.
- uniprot-2016 importedOn "2016-01-25" NP9743.RAk9NVJ0WE08oU6MvZSbmADwXQ4FJrQovlnD7RQ6-VUOY130_provenance.