@prefix vh8: <http://data.loterre.fr/ark:/67375/VH8> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .

vh8:-JFDJHJTQ-4
  skos:prefLabel "maladie congénitale"@fr, "congenital disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-MJMJNMFR-1 .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-MJMJNMFR-1 .

vh8:-MJMJNMFR-1
  skos:prefLabel "immunodéficit combiné sévère"@fr, "severe combined immunodeficiency"@en ;
  a skos:Concept ;
  skos:exactMatch <https://www.wikidata.org/wiki/Q1334408>, <https://en.wikipedia.org/wiki/Severe_combined_immunodeficiency> ;
  skos:broader vh8:-JFDJHJTQ-4, vh8:-N32K7HZ8-D, vh8:-MQ78NT00-6 ;
  skos:inScheme vh8: ;
  skos:definition "Severe combined immunodeficiency, SCID, is a rare genetic disorder characterized by the disturbed development of functional T cells and B cells caused by numerous genetic mutations that result in differing clinical presentations. (Wikipedia)"@en .

vh8:-MQ78NT00-6
  skos:prefLabel "immunodéficit"@fr, "immune deficiency"@en ;
  a skos:Concept ;
  skos:narrower vh8:-MJMJNMFR-1 .