This HTML5 document contains 49 embedded RDF statements represented using HTML+Microdata notation.

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

Namespace Prefixes

PrefixIRI
wdthttp://www.wikidata.org/prop/direct/
wdtnhttp://www.wikidata.org/prop/direct-normalized/
n11http://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#
n9http://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:Q54889350
rdf:type
wikibase:Item
p:P2888
wds:Q54889350-BB95923B-57BF-4D57-A9E8-18EE1521B627 wds:Q54889350-5EFCC09A-B96A-4C2E-9F8B-7DD29E1859AD
wdt:P2888
n9:Orphanet_2102 n9:Orphanet_238583
p:P5270
wds:Q54889350-72440ED7-EC13-46F9-96FC-DA52783D4866
wdtn:P5270
n11:MONDO_0009314
wdt:P5270
MONDO_0009314
rdfs:label
GTP cyclohydrolase I deficiency
skos:prefLabel
GTP cyclohydrolase I deficiency
schema:name
GTP cyclohydrolase I deficiency
p:P31
wds:Q54889350-8292C33B-82BE-404B-BBBD-1D88D3B1AA67 wds:Q54889350-66BC83CC-81CE-4159-A329-6FE43AFF9BD2
wdt:P31
wd:Q929833 wd:Q112193867
p:P279
wds:Q54889350-3da28aa1-420e-e6a1-3168-d8736ef035e1 wds:Q54889350-65f9216c-4208-5a87-ddb2-92df79d821f9
wdt:P279
wd:Q5898279 wd:Q239342
p:P11430
wds:Q54889350-2562e0b0-4f8d-4ded-369b-ee5b845a8c38
p:P1550
wds:Q54889350-A171FF55-3414-4425-82C7-00091CDD4D81
p:P2293
wds:Q54889350-43ED966F-4D30-4840-BC3E-BD5C64539E43
p:P4229
wds:Q54889350-3BF10C83-FE18-4DBD-BB19-2C3D5784B4C1
p:P4317
wds:Q54889350-BA5B1E83-65EF-4FF9-8DBB-2B506FD51FD1
p:P492
wds:Q54889350-1bae1088-4d12-96f4-b0bc-c30f84a8bd59 wds:Q54889350-689553E5-4417-414D-B0EF-1C9AA1B2084E
wdt:P11430
DI-00538
wdt:P1550
2102
wdt:P2293
wd:Q14916168
wdt:P4229
E70.1
wdt:P4317
2844
wdt:P492
233910
skos:altLabel
Hyperphenylalaninemia, Tetrahydrobiopterin-Deficient, Due to Gtp Cyclohydrolase 1 Deficiency Hyperphenylalaninemia, Bh4-Deficient, type B Dystonia, Dopa-Responsive, With or Without Hyperphenylalaninemia, Autosomal Recessive hyperphenylalaninemia, BH4-deficient, B Gtp Cyclohydrolase 1 Deficiency GTPCH deficiency HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B Hyperphenylalaninemia due to GTP cyclohydrolase deficiency HPABH4B BH4-deficient hyperphenylalaninemia B
p:P1748
wds:Q54889350-b42bd326-4cde-09fe-8309-4ce9d03e9f08 wds:Q54889350-D7ADC6EE-039B-4D59-AB46-CCC0D52E0F28
p:P2892
wds:Q54889350-F52FCE0A-038D-46C9-BFF4-59DD92808A4B wds:Q54889350-6D1AB92F-9BE4-48ED-8A0A-BED4DC7C8425
wdt:P1748
C141442
wdt:P2892
C0268467 C2673535