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About:
clgo:
MeSH_code_(C16)
Property
Value
rdf:
type
owl:
Class
rdfs:
label
MeSH code (C16)
rdfs:
subClassOf
owl:
Thing
prov:
wasDerivedFrom
http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16)
is
rdf:
type
of
Congenital rubella syndrome
Oculocerebrorenal syndrome
Spina bifida
Beta thalassemia
Maple syrup urine disease
Ehlers–Danlos syndromes
Cytochrome P450 oxidoreductase deficiency
Glycogen storage disease type VI
Fuchs' dystrophy
Marfan syndrome
Fetal hemoglobin
Cell (journal)
Choledochal cysts
Fragile X syndrome
Hemoglobin H disease
Mulibrey nanism
Leukodystrophy
Prader–Willi syndrome
Fabry disease
Multiple endocrine neoplasia type 2B
Hyperinsulinism-hyperammonemia syndrome
Ichthyosis vulgaris
Fanconi syndrome
Chondrodysplasia punctata
Duchenne
Congenital hypothyroidism
Lesch–Nyhan syndrome
Hartnup disease
Hypobetalipoproteinemia
Tourette syndrome
Tracheobronchomegaly
Goldenhar syndrome
Homocystinuria
Mucopolysaccharidosis
Carbamoyl phosphate synthetase I deficiency
Multiple hamartoma syndrome
Tuberous sclerosis
Factor VII deficiency
Tyrosinemia
WAGR syndrome
Alagille syndrome
Levocardia
Lip
Chronic granulomatous disease
Canavan disease
Hereditary spastic paraplegia
Galactosemia
Proteus syndrome
Tay–Sachs disease
Caroli disease
Dyskeratosis congenita
Nail–patella syndrome
Gangliosidosis
Klinefelter syndrome
Lipoprotein lipase deficiency
Rubinstein–Taybi syndrome
Apparent mineralocorticoid excess syndrome
Tetralogy of Fallot
Pseudoxanthoma elasticum
Nesidioblastosis
Tangier disease
Cleidocranial dysostosis
Dextrocardia
Myotonic dystrophy
Renal glycosuria
Hereditary elliptocytosis
Multiple endocrine neoplasia type 1
Pyruvate synthase
Ellis–Van Creveld syndrome
Hajdu–Cheney syndrome
Focal dermal hypoplasia
Gardner's syndrome
Dysostosis
Friedreich's ataxia
Down syndrome
Frasier syndrome
Hermansky–Pudlak syndrome
Hypolipoproteinemia
Menkes disease
Scimitar syndrome
Dandy–Walker malformation
Holoprosencephaly
Hyperhomocysteinemia
Turner syndrome
Alkaptonuria
Smith–Lemli–Opitz syndrome
Carbohydrate metabolism
Ichthyosis
Coffin–Lowry syndrome
Gaucher's disease
MELAS syndrome
Cherubism
Hereditary hyperbilirubinemia
Ebstein's anomaly
Haemochromatosis type 3
Mandibuloacral dysplasia
Porphyria
Atrophy
Laurence–Moon syndrome
Li–Fraumeni syndrome
... and more