sub:provenance {
  sub:assertion dcterms:description "[ALAD porphyria is a recessive disorder; there are two common variant ALAD alleles, which encode K59 and N59, and eight known porphyria-associated ALAD mutations, which encode F12L, E89K, C132R, G133R, V153M, R240W, A274T, and V275M.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    
wi:evidence dgn-void:source_evidence_curated ;
    
sio:SIO_000772 miriam-pubmed:17236137 ;
    
prov:wasDerivedFrom dgn-void:UNIPROT ;
    
prov:wasGeneratedBy eco:ECO_0000218 . 
  
dgn-void:UNIPROT pav:importedOn "2017-01-25"^^
xsd:date . 
  
dgn-void:source_evidence_curated a eco:ECO_0000205 ;
    
rdfs:comment "Gene-disease associations manually curated."@en ;
    
rdfs:label "DisGeNET evidence - CURATED"@en . 
}