@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:-MV1R3WNP-P
  skos:prefLabel "Cytogenetics"@en, "Cytogénétique"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-CS1KZF68-9 .

jvr:-WWJHCQRB-K
  skos:prefLabel "surgery (Qualifier)"@en, "chirurgie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-SDXQ5280-F
  skos:prefLabel "mortality (Qualifier)"@en, "mortalité (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-HPKB70N8-W
  skos:prefLabel "rehabilitation (Qualifier)"@en, "rééducation et réadaptation (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-V63LBLK0-6
  skos:prefLabel "Syndrome de Cornelia de Lange"@fr, "De Lange Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-VG20R78F-K
  skos:prefLabel "embryologie (Qualificatif)"@fr, "embryology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

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

jvr:-L6C0XPHT-4
  skos:prefLabel "métabolisme (Qualificatif)"@fr, "metabolism (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-WQ00QWRG-J
  skos:prefLabel "physiopathologie (Qualificatif)"@fr, "physiopathology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-DH7H9MJ2-N
  skos:prefLabel "anatomopathologie (Qualificatif)"@fr, "pathology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-MDQBX560-1
  skos:prefLabel "radiotherapy (Qualifier)"@en, "radiothérapie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-ZJBZVRWR-8
  skos:prefLabel "parasitologie (Qualificatif)"@fr, "parasitology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-W6T67RP3-2
  skos:prefLabel "diagnostic imaging (Qualifier)"@en, "imagerie diagnostique (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-B6C87218-T
  skos:prefLabel "prévention et contrôle (Qualificatif)"@fr, "prevention & control (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-TRWPPBQ0-H
  skos:prefLabel "Wolf-Hirschhorn Syndrome"@en, "Syndrome de Wolf-Hirschhorn"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-LLFZ7FD5-V
  skos:prefLabel "Syndrome de Beckwith-Wiedemann"@fr, "Beckwith-Wiedemann Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-BQ3W1P91-F
  skos:prefLabel "thérapie (Qualificatif)"@fr, "therapy (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-DZD0TKDJ-5
  skos:prefLabel "Syndrome branchio-oto-rénal"@fr, "Branchio-Oto-Renal Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-C1G4DPQT-C
  skos:prefLabel "Malformations"@fr, "Congenital Abnormalities"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-CS1KZF68-9 .

jvr:-KRXG97RR-5
  skos:prefLabel "diagnostic (Qualificatif)"@fr, "diagnosis (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-P56M5KRW-Z
  skos:prefLabel "Silver-Russell Syndrome"@en, "Syndrome de Silver-Russell"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-XL1NS8KF-X
  skos:prefLabel "Syndrome de Smith-Magenis"@fr, "Smith-Magenis Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-D3L2XS4S-G
  skos:prefLabel "Trisomy 13 Syndrome"@en, "Syndrome de Patau"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-B5NJWRD6-9
  skos:prefLabel "Syndrome de Jacobsen"@fr, "Jacobsen Distal 11q Deletion Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-J9Z93VFN-9
  skos:prefLabel "enzymology (Qualifier)"@en, "enzymologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-R490QF7F-9
  skos:prefLabel "Genetic Diseases, Inborn"@en, "Maladies génétiques congénitales"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-CS1KZF68-9 .

jvr:-X1MQPRW0-7
  skos:prefLabel "Williams Syndrome"@en, "Syndrome de Williams"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-T1QJHLQ4-J
  skos:prefLabel "microbiology (Qualifier)"@en, "microbiologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-KFM33PF8-L
  skos:prefLabel "médecine vétérinaire (Qualificatif)"@fr, "veterinary (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr: a skos:ConceptScheme .
jvr:-BBD0S71C-R
  skos:prefLabel "induit chimiquement (Qualificatif)"@fr, "chemically induced (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-XVHTZRCG-7
  skos:prefLabel "étiologie (Qualificatif)"@fr, "etiology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-SDPG013V-D
  skos:prefLabel "psychology (Qualifier)"@en, "psychologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-T6JZ48ZV-N
  skos:prefLabel "complications (Qualifier)"@en, "complications (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-P1X8SCQ6-K
  skos:prefLabel "virologie (Qualificatif)"@fr, "virology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-W6SQV79N-S
  skos:prefLabel "classification (Qualifier)"@en, "classification (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-GXVR9QN8-P
  skos:prefLabel "drug therapy (Qualifier)"@en, "traitement médicamenteux (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-RQM0BSS4-8
  skos:prefLabel "Chromosome Aberrations"@en, "Aberrations des chromosomes"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-CS1KZF68-9 .

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

jvr:-CB30NGKB-3
  skos:prefLabel "economics (Qualifier)"@en, "économie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-CBP4MS0V-K
  skos:prefLabel "Down Syndrome"@en, "Syndrome de Down"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-K3L5GLNL-M
  skos:prefLabel "Syndrome d'Angelman"@fr, "Angelman Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-BT300B3G-Q
  skos:prefLabel "cerebrospinal fluid (Qualifier)"@en, "liquide cérébrospinal (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-CSKTXWF5-F
  skos:prefLabel "epidemiology (Qualifier)"@en, "épidémiologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-JVKFK2NX-2
  skos:prefLabel "nursing (Qualifier)"@en, "soins infirmiers (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-MZCJWN7K-G
  skos:prefLabel "Syndrome WAGR"@fr, "WAGR Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-W4X1LN61-R
  skos:prefLabel "diet therapy (Qualifier)"@en, "diétothérapie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-K6WT37LH-3
  skos:prefLabel "Syndrome de Prader-Willi"@fr, "Prader-Willi Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-B8PBJMT7-G
  skos:prefLabel "Genetics, Medical"@en, "Génétique médicale"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-CS1KZF68-9 .

jvr:-CWFFHX6H-P
  skos:prefLabel "22q11 Deletion Syndrome"@en, "Syndrome de délétion 22q11"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-WM8ZHH7V-W
  skos:prefLabel "Rubinstein-Taybi Syndrome"@en, "Syndrome de Rubinstein-Taybi"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-QWPJH3S1-Q
  skos:prefLabel "Maladies liées aux chromosomes sexuels"@fr, "Sex Chromosome Disorders"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-RC3PND0F-S
  skos:prefLabel "ethnology (Qualifier)"@en, "ethnologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-XV06LPML-W
  skos:prefLabel "urine (Qualifier)"@en, "urine (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-GKT5SJTB-G
  skos:prefLabel "Syndrome d'Edwards"@fr, "Trisomy 18 Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-SKFX7SK9-9
  skos:prefLabel "Holoprosencéphalie"@fr, "Holoprosencephaly"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-CS1KZF68-9
  mesh:allowableQualifier jvr:-SDPG013V-D, jvr:-GXVR9QN8-P, jvr:-SDXQ5280-F, jvr:-W4X1LN61-R, jvr:-KFM33PF8-L, jvr:-CSKTXWF5-F, jvr:-P1X8SCQ6-K, jvr:-SBNWSM1T-R, jvr:-NHL3D2X0-S, jvr:-S0CS1X5R-5, jvr:-HPKB70N8-W, jvr:-Z9TSGBXH-4, jvr:-JVKFK2NX-2, jvr:-DH7H9MJ2-N, jvr:-T1QJHLQ4-J, jvr:-RC3PND0F-S, jvr:-ZJBZVRWR-8, jvr:-MDQBX560-1, jvr:-CB30NGKB-3, jvr:-B6C87218-T, jvr:-L6C0XPHT-4, jvr:-BBD0S71C-R, jvr:-XV06LPML-W, jvr:-BQ3W1P91-F, jvr:-J9Z93VFN-9, jvr:-KRXG97RR-5, jvr:-BT300B3G-Q, jvr:-T6JZ48ZV-N, jvr:-WQ00QWRG-J, jvr:-WWJHCQRB-K, jvr:-VG20R78F-K, jvr:-W6T67RP3-2, jvr:-XVHTZRCG-7, jvr:-W6SQV79N-S ;
  skos:narrower jvr:-D3L2XS4S-G, jvr:-K6WT37LH-3, jvr:-TRWPPBQ0-H, jvr:-DZD0TKDJ-5, jvr:-LLFZ7FD5-V, jvr:-WM8ZHH7V-W, jvr:-GKT5SJTB-G, jvr:-B5NJWRD6-9, jvr:-P56M5KRW-Z, jvr:-CWFFHX6H-P, jvr:-V63LBLK0-6, jvr:-K3L5GLNL-M, jvr:-XL1NS8KF-X, jvr:-CBP4MS0V-K, jvr:-QWPJH3S1-Q, jvr:-L1KQNJR9-L, jvr:-LS9LF2W0-C, jvr:-MZCJWN7K-G, jvr:-X1MQPRW0-7, jvr:-SKFX7SK9-9 ;
  skos:broader jvr:-C1G4DPQT-C, jvr:-R490QF7F-9 ;
  skos:hiddenLabel "Maladies autosomiques"@fr, "Autosomal Chromosome Disorders"@en, "Maladies chromosomiques autosomiques"@fr, "Troubles autosomiques"@fr ;
  dc:created "2001-07-25"^^xsd:date ;
  skos:altLabel "Chromosome Abnormality Disorders"@en, "Chromosomal Disorders"@en, "Maladies par aberrations chromosomiques"@fr, "Troubles chromosomiques"@fr ;
  dc:modified "2009-07-06"^^xsd:date ;
  skos:inScheme jvr: ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-RQM0BSS4-8, jvr:-B8PBJMT7-G, jvr:-MV1R3WNP-P ;
  skos:prefLabel "Maladies chromosomiques"@fr, "Chromosome Disorders"@en ;
  owl:sameAs <http://id.nlm.nih.gov/mesh/D025063> ;
  skos:definition "Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material (either a whole chromosome or a chromosome segment). (from Thompson et al., Genetics in Medicine, 5th ed, p429)"@en ;
  dc:established "2002-01-01"^^xsd:date .

jvr:-NHL3D2X0-S
  skos:prefLabel "sang (Qualificatif)"@fr, "blood (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-L1KQNJR9-L
  skos:prefLabel "Syndrome de Sotos"@fr, "Sotos Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-LS9LF2W0-C
  skos:prefLabel "Cri-du-Chat Syndrome"@en, "Maladie du cri du chat"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-CS1KZF68-9 .

jvr:-SBNWSM1T-R
  skos:prefLabel "history (Qualifier)"@en, "histoire (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .