@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:-H84N3XTH-1
  skos:prefLabel "Aniridie"@fr, "Aniridia"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

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:-C614PBSR-M
  skos:prefLabel "Rétinoblastome"@fr, "Retinoblastoma"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

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

jvr:-QCC3H5R1-3
  skos:prefLabel "Amaurose congénitale de Leber"@fr, "Leber Congenital Amaurosis"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

jvr:-NNF6WD0C-X
  skos:prefLabel "Aicardi Syndrome"@en, "Syndrome d'Aicardi"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

jvr:-RBXH1300-0
  skos:prefLabel "Optic Atrophies, Hereditary"@en, "Atrophies optiques héréditaires"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

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

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

jvr:-K4LKB9DG-W
  skos:prefLabel "Syndrome de Weill-Marchesani"@fr, "Weill-Marchesani Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

jvr:-KQG0FKCK-3
  skos:prefLabel "Choroïdérémie"@fr, "Choroideremia"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

jvr:-R0FNLV2B-2
  mesh:allowableQualifier jvr:-VG20R78F-K, jvr:-Z9TSGBXH-4, jvr:-WWJHCQRB-K, jvr:-XV06LPML-W, jvr:-W6T67RP3-2, jvr:-KRXG97RR-5, jvr:-BBD0S71C-R, jvr:-T6JZ48ZV-N, jvr:-DH7H9MJ2-N, jvr:-W4X1LN61-R, jvr:-CSKTXWF5-F, jvr:-ZJBZVRWR-8, jvr:-GXVR9QN8-P, jvr:-RC3PND0F-S, jvr:-W6SQV79N-S, jvr:-WQ00QWRG-J, jvr:-SDXQ5280-F, jvr:-BT300B3G-Q, jvr:-HPKB70N8-W, jvr:-SBNWSM1T-R, jvr:-B6C87218-T, jvr:-CB30NGKB-3, jvr:-L6C0XPHT-4, jvr:-SDPG013V-D, jvr:-KFM33PF8-L, jvr:-XVHTZRCG-7, jvr:-JVKFK2NX-2, jvr:-S0CS1X5R-5, jvr:-T1QJHLQ4-J, jvr:-P1X8SCQ6-K, jvr:-BQ3W1P91-F, jvr:-NHL3D2X0-S, jvr:-J9Z93VFN-9, jvr:-MDQBX560-1 ;
  dc:established "1990-01-01"^^xsd:date ;
  skos:prefLabel "Maladies héréditaires de l'oeil"@fr, "Eye Diseases, Hereditary"@en ;
  skos:narrower jvr:-RGPFZ7JN-T, jvr:-CLGL8JB7-3, jvr:-M24WLQC0-Q, jvr:-H84N3XTH-1, jvr:-KQG0FKCK-3, jvr:-K4LKB9DG-W, jvr:-WV1FCHDS-H, jvr:-MPVSD7Z4-2, jvr:-RBXH1300-0, jvr:-R3HSQCFQ-F, jvr:-DNSS68FX-F, jvr:-SP3P0HLW-P, jvr:-C614PBSR-M, jvr:-K3536N0G-D, jvr:-NNF6WD0C-X, jvr:-S3QHFCVZ-C, jvr:-W6GN27VN-H, jvr:-QCC3H5R1-3, jvr:-B04D47W1-Z ;
  dc:modified "2019-06-17"^^xsd:date ;
  skos:altLabel "Hereditary Eye Diseases"@en, "Maladie héréditaire de l'oeil"@fr, "Maladies héréditaires des yeux"@fr, "Maladies oculaires héréditaires"@fr ;
  skos:broader jvr:-QSC0SW7L-8, jvr:-R490QF7F-9 ;
  owl:sameAs <http://id.nlm.nih.gov/mesh/D015785> ;
  a skos:Concept, mesh:Descriptor ;
  dc:created "1989-09-06"^^xsd:date ;
  skos:inScheme jvr: ;
  skos:definition "Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder."@en .

jvr:-B04D47W1-Z
  skos:prefLabel "Coloboma"@en, "Colobome"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

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:-R0FNLV2B-2 .

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:-CLGL8JB7-3
  skos:prefLabel "Dystrophie des cônes"@fr, "Cone Dystrophy"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

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:-S3QHFCVZ-C
  skos:prefLabel "Graves Ophthalmopathy"@en, "Ophtalmopathie basedowienne"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

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:-M24WLQC0-Q
  skos:prefLabel "Atrophie gyrée"@fr, "Gyrate Atrophy"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

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:-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:-K3536N0G-D
  skos:prefLabel "Walker-Warburg Syndrome"@en, "Syndrome de Walker-Warburg"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

jvr:-SP3P0HLW-P
  skos:prefLabel "Dystrophies héréditaires de la cornée"@fr, "Corneal Dystrophies, Hereditary"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

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:-QSC0SW7L-8
  skos:prefLabel "Eye Diseases"@en, "Maladies de l'oeil"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-R0FNLV2B-2 .

jvr:-DNSS68FX-F
  skos:prefLabel "Albinisme"@fr, "Albinism"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

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

jvr:-RGPFZ7JN-T
  skos:prefLabel "Dégénérescence de la rétine"@fr, "Retinal Degeneration"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

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

jvr:-WV1FCHDS-H
  skos:prefLabel "Dysplasie rétinienne"@fr, "Retinal Dysplasia"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

jvr:-MPVSD7Z4-2
  skos:prefLabel "Vitréorétinopathies exsudatives familiales"@fr, "Familial Exudative Vitreoretinopathies"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

jvr:-R3HSQCFQ-F
  skos:prefLabel "Duane Retraction Syndrome"@en, "Syndrome de rétraction de Duane"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .

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

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

jvr:-W6GN27VN-H
  skos:prefLabel "Optic Nerve Hypoplasia"@en, "Hypoplasie du nerf optique"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-R0FNLV2B-2 .