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

vh8: a skos:ConceptScheme .
vh8:-QG1RVCT9-L
  skos:prefLabel "complex syndrome"@en, "syndrome complexe"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-P35S155W-4 .

vh8:-K74MDW6H-R
  skos:prefLabel "craniosynostose"@fr, "craniosynostosis"@en ;
  a skos:Concept ;
  skos:narrower vh8:-P35S155W-4 .

vh8:-P35S155W-4
  skos:definition "Craniofrontonasal dysplasia (craniofrontonasal syndrome, craniofrontonasal dysostosis, CFND) is a very rare X-linked malformation syndrome caused by mutations in the ephrin-B1 gene (EFNB1). (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-K74MDW6H-R, vh8:-QG1RVCT9-L ;
  skos:prefLabel "syndrome craniofrontonasal"@fr, "craniofrontonasal syndrome"@en ;
  skos:exactMatch <https://www.wikidata.org/wiki/Q5182141>, <https://en.wikipedia.org/wiki/Craniofrontonasal_dysplasia> .