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

vh8: a skos:ConceptScheme .
vh8:-F0Q8HP18-R
  skos:prefLabel "malformation"@fr, "malformation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-L6SV38VN-C .

vh8:-L6SV38VN-C
  skos:exactMatch <https://en.wikipedia.org/wiki/Blepharophimosis>, <https://www.wikidata.org/wiki/Q883850> ;
  a skos:Concept ;
  skos:prefLabel "blépharophimosis"@fr, "blepharophimosis"@en ;
  skos:inScheme vh8: ;
  skos:broader vh8:-F5343M6M-C, vh8:-F0Q8HP18-R ;
  skos:definition "Blepharophimosis is a congenital condition characterized by a horizontally narrow palpebral fissure. It is also part of a syndrome blepharophimosis, ptosis, and epicanthus inversus syndrome, also called blepharophimosis syndrome, which is a condition where the patient has bilateral ptosis with reduced lid size, vertically and horizontally. (Wikipedia)"@en ;
  skos:altLabel "epicanthus inversus"@fr .

vh8:-F5343M6M-C
  skos:prefLabel "eyelid disease"@en, "pathologie de la paupière"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-L6SV38VN-C .