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

vh8:-K9M0X8PR-C
  skos:prefLabel "anémie aplasique"@fr, "aplastic anemia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-W8K8J6P8-3 .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-W8K8J6P8-3 .

vh8:-Z080LN2C-5
  skos:prefLabel "chromosome fragility"@en, "fragilité chromosomique"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-W8K8J6P8-3 .

vh8:-W8K8J6P8-3
  a skos:Concept ;
  skos:broader vh8:-K9M0X8PR-C, vh8:-Z080LN2C-5, vh8:-N32K7HZ8-D ;
  skos:inScheme vh8: ;
  skos:altLabel "anémie aplasique essentielle de type Fanconi"@fr ;
  skos:prefLabel "anémie de Fanconi"@fr, "Fanconi anemia"@en ;
  skos:exactMatch <https://www.wikidata.org/wiki/Q845779>, <https://fr.wikipedia.org/wiki/An%C3%A9mie_de_Fanconi>, <https://en.wikipedia.org/wiki/Fanconi_anemia> ;
  skos:definition "Fanconi anaemia (FA) is a rare genetic disease resulting in impaired response to DNA damage. Although it is a very rare disorder, study of this and other bone marrow failure syndromes has improved scientific understanding of the mechanisms of normal bone marrow function and development of cancer. (Wikipedia)"@en, "L’anémie de Fanconi est une maladie génétique rare faisant partie des syndromes d'insuffisance médullaire héréditaires (en anglais : Inherited Bone Marrow Failure syndromes). (Wikipédia)"@fr .