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About:
clgo:
Channelopathie
Property
Value
rdf:
type
owl:
Class
rdfs:
label
Channelopathie
rdfs:
subClassOf
Disease
prov:
wasDerivedFrom
http://en.wikipedia.org/wiki/Category:Channelopathies
is
rdf:
type
of
Hemiplegic migraine
Long QT syndrome
Familial hemiplegic migraine
Hyperkalemic periodic paralysis
Autoimmune autonomic ganglionopathy
Paroxysmal extreme pain disorder
Juvenile myoclonic epilepsy
Pseudohypoaldosteronism
Romano–Ward syndrome
Retinitis pigmentosa
Focal segmental glomerulosclerosis
Generalized epilepsy with febrile seizures plus
Sporadic hemiplegic migraine
Posterior column ataxia-retinitis pigmentosa syndrome
Malignant hyperthermia
Benign familial neonatal seizures
Autosomal dominant polycystic kidney disease
Congenital stationary night blindness
Bartter syndrome
Rolandic epilepsy
Potassium-aggravated myotonia
Lambert–Eaton myasthenic syndrome
Nonsyndromic deafness
Calciumopathy
Congenital hyperinsulinism
Congenital insensitivity to pain
Channelome
Autosomal dominant nocturnal frontal lobe epilepsy
Childhood absence epilepsy
Episodic ataxia
Paramyotonia congenita
Timothy syndrome
Catecholaminergic polymorphic ventricular tachycardia
Cystic fibrosis
Familial atrial fibrillation
Short QT syndrome
Spinocerebellar ataxia type-13
Periodic paralysis
Spinocerebellar ataxia type 6
Mucolipidosis type IV
Dent's disease
Erythromelalgia
Myotonia congenita
Achromatopsia
Hypomagnesemia with secondary hypocalcemia
Andersen–Tawil syndrome
Brugada syndrome
Channelopathy
Hypokalemic periodic paralysis
Maculopathy