This HTML5 document contains 40 embedded RDF statements represented using HTML+Microdata notation.

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PrefixNamespace IRI
n10http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C18)
n16http://caligraph.org/ontology/MeSH_code_(C18)
rdfshttp://www.w3.org/2000/01/rdf-schema#
n7http://en.wikipedia.org/wiki/List_of_diseases_(T)
n12http://en.wikipedia.org/wiki/Category:
skoshttp://www.w3.org/2004/02/skos/core#
n13http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16)
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n15http://caligraph.org/ontology/MeSH_code_(C16)
owlhttp://www.w3.org/2002/07/owl#
n9http://en.wikipedia.org/wiki/List_of_diseases_(O)
clgohttp://caligraph.org/ontology/
n8http://en.wikipedia.org/wiki/
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xsdhhttp://www.w3.org/2001/XMLSchema#
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clgrhttp://caligraph.org/resource/
Subject Item
clgr:Tyrosinemia
rdf:type
clgo:Skin_condition clgo:Cause_of_hypoglycemia clgo:Autosomal_recessive_disorder clgo:Amino_acid_metabolism_disorder owl:NamedIndividual n15: n16: clgo:Disorder_included_in_newborn_screening_programs
rdfs:label
Tyrosinemia
owl:sameAs
dbr:Tyrosinemia
prov:wasDerivedFrom
n7: n8:Proximal_renal_tubular_acidosis n9: n10: n8:Chromosome_15 n8:Chromosome_12 n8:Congenital_disorders_of_amino_acid_metabolism n8:Keratoderma n8:List_of_causes_of_hypoglycemia n12:Amino_acid_metabolism_disorders n8:List_of_disorders_included_in_newborn_screening_programs n13: n12:Autosomal_recessive_disorders
skos:prefLabel
Tyrosinemia
skos:altLabel
tyrosinemias Oculocutaneous tyrosinemia hereditary tyrosinemia type I Tyrosinemia I hereditary tyrosinemia type 1 Tyrosinemia III Tyrosinaemia type 1 Tyrosine-oxidase temporary deficiency tyrosinemia
clgo:diseasesDB
13478
clgo:eMedicineSubject
ped
clgo:eMedicineTopic
2339
clgo:icd10
E70.2
clgo:icd9
270.2
clgo:meshId
D020176
clgo:omim
276700