@prefix jvr: <http://data.loterre.fr/ark:/67375/JVR> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix mesh: <http://id.nlm.nih.gov/mesh/vocab#> .
@prefix dc: <http://purl.org/dc/terms/> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .

jvr:-Z9TSGBXH-4
  skos:prefLabel "génétique (Qualificatif)"@fr, "genetics (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-H7K65Q8S-Z
  skos:prefLabel "radiation effects (Qualifier)"@en, "effets des radiations (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-NT58TNXQ-G
  skos:prefLabel "Trinucleotide Repeat Expansion"@en, "Expansion de trinucléotide répété"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-CGT2SN12-T .

jvr:-S0CS1X5R-5
  skos:prefLabel "immunology (Qualifier)"@en, "immunologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-NRV3FDLW-5
  skos:prefLabel "Chromosomal Instability"@en, "Instabilité des chromosomes"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-CGT2SN12-T .

jvr:-N2WP45CN-V
  skos:prefLabel "drug effects (Qualifier)"@en, "effets des médicaments et des substances chimiques (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-KZK3R3W2-V
  skos:prefLabel "Fragile X Syndrome"@en, "Syndrome du chromosome X fragile"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-CGT2SN12-T .

jvr:-MLKJS7X2-4
  skos:prefLabel "DNA Sequence, Unstable"@en, "Séquence instable d'ADN"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-CGT2SN12-T .

jvr:-PPKJKFKK-V
  skos:prefLabel "ethics (Qualifier)"@en, "éthique (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-CGT2SN12-T
  skos:related jvr:-MLKJS7X2-4, jvr:-VWVSVF45-N, jvr:-MLD02K7C-B, jvr:-C0TW4VR1-Z, jvr:-KZK3R3W2-V, jvr:-NT58TNXQ-G ;
  mesh:allowableQualifier jvr:-N2WP45CN-V, jvr:-H7K65Q8S-Z, jvr:-PPKJKFKK-V, jvr:-Z9TSGBXH-4, jvr:-WZF2ZR3L-B, jvr:-S0CS1X5R-5 ;
  skos:definition "Susceptibility of chromosomes to breakage leading to translocation; CHROMOSOME INVERSION; SEQUENCE DELETION; or other CHROMOSOME BREAKAGE related aberrations."@en ;
  skos:inScheme jvr: ;
  skos:broader jvr:-NRV3FDLW-5 ;
  dc:created "1981-02-23"^^xsd:date ;
  dc:established "1982-01-01"^^xsd:date ;
  owl:sameAs <http://id.nlm.nih.gov/mesh/D002873> ;
  a mesh:Descriptor, skos:Concept ;
  skos:prefLabel "Fragilité des chromosomes"@fr, "Chromosome Fragility"@en ;
  skos:altLabel "Fragilité chromosomique"@fr, "Chromosomal Fragility"@en ;
  dc:modified "2008-07-08"^^xsd:date .

jvr:-MLD02K7C-B
  skos:prefLabel "Expansion de séquence répétée de l'ADN"@fr, "DNA Repeat Expansion"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-CGT2SN12-T .

jvr:-C0TW4VR1-Z
  skos:prefLabel "Cassure de chromosome"@fr, "Chromosome Breakage"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-CGT2SN12-T .

jvr:-WZF2ZR3L-B
  skos:prefLabel "physiology (Qualifier)"@en, "physiologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr: a skos:ConceptScheme .
jvr:-VWVSVF45-N
  skos:prefLabel "Sites fragiles de chromosome"@fr, "Chromosome Fragile Sites"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-CGT2SN12-T .