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About:
clgr:
CAPOS_syndrome
Property
Value
rdf:
type
owl:
NamedIndividual
Autosomal dominant disorder
Rare genetic syndrome
Syndrome with sensorineural hearing loss
Episodic and paroxysmal disorder
Syndrome affecting the optic nerve
rdfs:
label
CAPOS syndrome
owl:
sameAs
dbr:
CAPOS_syndrome
prov:
wasDerivedFrom
http://en.wikipedia.org/wiki/Category:Autosomal_dominant_disorders
http://en.wikipedia.org/wiki/Category:Rare_genetic_syndromes
http://en.wikipedia.org/wiki/Category:Syndromes_with_sensorineural_hearing_loss
http://en.wikipedia.org/wiki/Category:Episodic_and_paroxysmal_disorders
http://en.wikipedia.org/wiki/Category:Syndromes_affecting_the_optic_nerve
skos:
prefLabel
CAPOS syndrome
skos:
altLabel
CAPOS/CAOS syndrome
clgo:
alias
CAPOS
CAPOS syndrome. Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome. Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss.