This HTML5 document contains 55 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
wdthttp://www.wikidata.org/prop/direct/
wdtnhttp://www.wikidata.org/prop/direct-normalized/
n13http://purl.obolibrary.org/obo/
schemahttp://schema.org/
rdfshttp://www.w3.org/2000/01/rdf-schema#
skoshttp://www.w3.org/2004/02/skos/core#
wikibasehttp://wikiba.se/ontology#
phttp://www.wikidata.org/prop/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n6http://purl.obolibrary.org/obo/DOID_DOID:
n14http://identifiers.org/doid/DOID:
n8http://www.orpha.net/ORDO/
xsdhhttp://www.w3.org/2001/XMLSchema#
wdshttp://www.wikidata.org/entity/statement/
wdhttp://www.wikidata.org/entity/

Statements

Subject Item
wd:Q32143535
rdf:type
wikibase:Item
schema:description
Usher syndrome type 1 that has material basis in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22
p:P2888
wds:Q32143535-E4DFBC1E-7CAE-4091-A91E-73ECD3D9232A wds:Q32143535-E9DDD1CC-D649-42ED-88FA-FA1F0FBCAA95 wds:Q32143535-3AC60AD2-4A7D-465B-B1EC-F6570FFDC7A5 wds:Q32143535-B2A251A5-7356-4FCC-BDFF-7BD561248552
wdt:P2888
n8:Orphanet_231169 n8:Orphanet_886 n14:0110831 n13:DOID_0110831
p:P5270
wds:Q32143535-D6162BE1-B63B-4E65-8301-4E2D83689510
p:P699
wds:Q32143535-2A8E7E48-B3A7-4805-B392-193D9CEA0BC8
wdtn:P5270
n13:MONDO_0010984
wdtn:P699
n6:0110831
wdt:P5270
MONDO_0010984
wdt:P699
DOID:0110831
rdfs:label
Usher syndrome type 1D
skos:prefLabel
Usher syndrome type 1D
schema:name
Usher syndrome type 1D
p:P31
wds:Q32143535-C05A9261-2D67-4AEA-BE14-2C10334ECC3E wds:Q32143535-C9D32527-218D-47F0-A6C4-E40F2DA74041
wdt:P31
wd:Q929833 wd:Q112193867
p:P279
wds:Q32143535-6D272DD3-2B34-4347-B286-293FBECB1404 wds:Q32143535-48A533F2-79A2-4F13-BC21-DF5F48CA9723
wdt:P279
wd:Q66299868 wd:Q32143464
p:P11430
wds:Q32143535-86b72c75-4881-2cf2-d480-377a91cc2feb
p:P2293
wds:Q32143535-CFC055BB-659B-42AF-AB0B-150D97C74EA0 wds:Q32143535-102292C6-FEB8-48D7-B6E7-861B5E790276
p:P4229
wds:Q32143535-87FD91B5-AC4C-45EA-B7A8-845B79779684
p:P4317
wds:Q32143535-6993B4A4-5E8C-4B78-A36E-9701CFF303B4
p:P492
wds:Q32143535-69D207FF-DEC2-443F-8484-82B00E450347 wds:Q32143535-D2519BAB-8F66-4A43-A745-E58E34BD4FDE
wdt:P11430
DI-01114
wdt:P2293
wd:Q18045544 wd:Q18045862
wdt:P4229
H35.5
wdt:P4317
5438
wdt:P492
601067
skos:altLabel
USHER SYNDROME, TYPE ID USH1D Usher Syndrome, Type Id/F, Cdh23/Pcdh15, Digenic Usher syndrome type ID USHER SYNDROME, TYPE ID; USH1D Ush1D/F, Cdh23/Pcdh15, Digenic Usher syndrome, type 1D
p:P2892
wds:Q32143535-1AAD59C3-90A3-4D51-A033-003C9EC3627C wds:Q32143535-90D3D128-770F-4D47-B4B5-1E894CEC7821 wds:Q32143535-C9AC5C16-0FA5-4961-A867-6BA4CFFAC8A9
p:P5008
wds:Q32143535-6010ABCD-51D7-4FD3-8E90-FEE84FBA583E
wdt:P2892
C3152102 C3275872 C1832845
wdt:P5008
wd:Q4099686