This HTML5 document contains 62 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

PrefixNamespace IRI
n13http://caligraph.org/resource/John%20Tracy_(18834482)
n17http://caligraph.org/resource/Katie_Kelly_(paratriathlete)
n4http://en.wikipedia.org/wiki/Mohr%E2%80%93Tranebj%C3%A6
n19http://caligraph.org/resource/Vendon%20Wright_(23906203)
n15http://caligraph.org/resource/Rachel%20Chaikof_(23961804)
n8http://en.wikipedia.org/wiki/List_of_diseases_(U)
rdfshttp://www.w3.org/2000/01/rdf-schema#
n12http://en.wikipedia.org/wiki/Category:
n20http://caligraph.org/resource/Christian%20Markovic_(22614267)
skoshttp://www.w3.org/2004/02/skos/core#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
n18http://caligraph.org/resource/Robert%20Tarango_(18249978)
clgohttp://caligraph.org/ontology/
n6http://en.wikipedia.org/wiki/
provhttp://www.w3.org/ns/prov#
xsdhhttp://www.w3.org/2001/XMLSchema#
n14http://caligraph.org/resource/Christine%20%22Coco%22%20Roschaert_(19076772)
n16http://caligraph.org/resource/James%20D.%20Watson_(21153514)
dbrhttp://dbpedia.org/resource/
clgrhttp://caligraph.org/resource/
Subject Item
n16:
clgo:deathCause
clgr:Usher_syndrome
Subject Item
n17:
clgo:deathCause
clgr:Usher_syndrome
Subject Item
clgr:Maria_Bitner-Glindzicz
clgo:academicDiscipline
clgr:Usher_syndrome
Subject Item
clgr:Teigan_Van_Roosmalen
clgo:deathCause
clgr:Usher_syndrome
Subject Item
clgr:Rebecca_Alexander
clgo:deathCause
clgr:Usher_syndrome
Subject Item
n20:
clgo:deathCause
clgr:Usher_syndrome
Subject Item
n13:
clgo:deathCause
clgr:Usher_syndrome
Subject Item
n18:
clgo:deathCause
clgr:Usher_syndrome
Subject Item
clgr:Cyril_Axelrod
clgo:deathCause
clgr:Usher_syndrome
Subject Item
clgr:Usher_syndrome
rdf:type
clgo:Ashkenazi_Jews_topic owl:NamedIndividual clgo:Rare_disease clgo:Syndrome clgo:Autosomal_recessive_disorder clgo:Disease_of_the_ear_and_mastoid_process clgo:Cytoskeletal_defect
rdfs:label
Usher syndrome
owl:sameAs
dbr:Usher_syndrome
prov:wasDerivedFrom
n4:rg_syndrome n6:Chromosome_1 n6:Chromosome_3 n6:Photosensitivity_in_humans n6:Chromosome_5 n6:Electroretinography n8: n6:Enamel_hypoplasia n6:Chromosome_17 n12:Rare_diseases n6:Usher_1C n6:Human_genome n12:Syndromes n6:Finnish_heritage_disease n12:Syndromes_by_cause n12:Syndromes_by_affected_organ n12:Ashkenazi_Jews_topics n6:Chromosome_11 n6:Deafblindness n6:Congenital_hyperinsulinism n6:Hearing_Health_Foundation n12:Cytoskeletal_defects n6:Chromosome_10 n6:List_of_syndromes n12:Autosomal_recessive_disorders n6:Vision_Institute n6:Medical_genetics_of_Jews n12:Diseases_of_the_ear_and_mastoid_process
skos:prefLabel
Usher syndrome
skos:altLabel
usher syndrome Usher syndrome type II Usher syndrome network Usher Syndrome Usher Usher 1 syndromes
clgo:diseasesDB
13611
clgo:icd10
H35.53
clgo:meshId
D052245
clgo:omim
276900
clgo:orpha
886
Subject Item
clgr:Catherine_Fischer
clgo:deathCause
clgr:Usher_syndrome
Subject Item
n14:
clgo:deathCause
clgr:Usher_syndrome
Subject Item
n15:
clgo:deathCause
clgr:Usher_syndrome
Subject Item
n19:
clgo:deathCause
clgr:Usher_syndrome