CaLiGraph
Formats
RDF
N-Triples
N3/Turtle
JSON
XML
CSV
OData
Atom
JSON
Microdata
JSON
HTML
Embedded
JSON
Turtle
Browse using
OpenLink Faceted Browser
OpenLink Structured Data Editor
LodLive Browser
LODmilla Browser
Sparql Endpoint
About:
clgr:
Syndactyly-nystagmus_syndrome_due_to_2q31.1_microduplication
Property
Value
rdf:
type
owl:
NamedIndividual
Autosomal dominant disorder
Rare genetic syndrome
Autosomal duplication
rdfs:
label
Syndactyly-nystagmus syndrome due to 2q31.1 microduplication
owl:
sameAs
dbr:
Syndactyly-nystagmus_syndrome_due_to_2q31.1_microduplication
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:Autosomal_duplications
skos:
prefLabel
Syndactyly-nystagmus syndrome due to 2q31.1 microduplication
clgo:
alias
2q31.1 microduplication syndrome