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

vh8:-J7B2408T-G
  skos:prefLabel "sinusite"@fr, "sinusitis"@en ;
  a skos:Concept ;
  skos:narrower vh8:-ZWW7QBD6-G .

vh8:-SNWNQ8G6-M
  skos:prefLabel "stérilité"@fr, "sterility"@en ;
  a skos:Concept ;
  skos:narrower vh8:-ZWW7QBD6-G .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-ZWW7QBD6-G .

vh8:-ZWW7QBD6-G
  skos:altLabel "syndrome de Kartagener"@fr, "syndrome d'immotilité ciliaire"@fr ;
  skos:prefLabel "immotile cilia syndrome"@en, "syndrome du cil immobile"@fr ;
  skos:broader vh8:-N32K7HZ8-D, vh8:-J7B2408T-G, vh8:-F7TMP9RK-4, vh8:-SNWNQ8G6-M ;
  a skos:Concept ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Primary_ciliary_dyskinesia> ;
  skos:definition "Primary ciliary dyskinesia (PCD), is a rare, ciliopathic, autosomal recessive genetic disorder that causes defects in the action of cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear), fallopian tube, and flagellum of sperm cells. (Wikipedia)"@en ;
  skos:inScheme vh8: .

vh8:-F7TMP9RK-4
  skos:prefLabel "infection respiratoire"@fr, "respiratory system infection"@en ;
  a skos:Concept ;
  skos:narrower vh8:-ZWW7QBD6-G .