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rdfs:label
|
"Tirosinemia"@es
"Tirozinemija"@bs
"Tyrosinemia"@fi
"Tyrosinämie"@de
"Tyrozynemia"@pl
"tirosinemia"@it
"tirosinemia"@pt
"tyrosinemi"@nn
"tyrosinemia"@en
"tyrosinemie"@nl
"tyrosinémie"@fr
"Наследна Тироцинемија"@mk
"Тирозинемия"@ru
"Тирозинемија"@sr
"تیروزینمی"@fa
"فرط تيروزين الدم"@ar
"チロシン血症"@ja
"酪胺酸血症"@zh
"酪胺酸血症"@zh-cn
"酪胺酸血症"@zh-hans
"酪胺酸血癥"@zh-hant
"티로신혈증"@ko
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|
skos:altLabel
|
"Disorder of tyrosine metabolism"@en
"原发性酪氨酸血症"@zh
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schema:description
|
"Condición médica"@es
"Krankheit"@de
"amino acid metabolic disorder that involves impaired break down of the amino acid tyrosine"@en
"groupe de maladies"@fr
"malattia metabolica congenita, in cui il corpo non riesce a metabolizzare l'amminoacido tirosina"@it
"recesywna choroba genetyczna"@pl
"хвороба"@uk
"질병의 종류"@ko
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schema:dateModified
|
"2026-10-23T23:57:04+00:00"^^xsd:dateTime
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schema:version
|
2560160613
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wikibase:identifiers
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32
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34
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wikibase:sitelinks
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17
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wikibase:statements
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50
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p:direct-normalized/P486
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<http://id.nlm.nih.gov/mesh/D020176>
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p:direct-normalized/P5270
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<http://purl.obolibrary.org/obo/MONDO_0017307>
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p:direct-normalized/P6366
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<https://makg.org/entity/2781097277>
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p:direct-normalized/P665
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<http://www.kegg.jp/entry/H00165>
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p:direct-normalized/P672
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<http://id.nlm.nih.gov/mesh/C10.228.140.163.100.875>
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<http://id.nlm.nih.gov/mesh/C16.320.565.100.880>
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<http://id.nlm.nih.gov/mesh/C16.320.565.189.875>
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<http://id.nlm.nih.gov/mesh/C18.452.132.100.875>
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<http://id.nlm.nih.gov/mesh/C18.452.648.100.880>
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<http://id.nlm.nih.gov/mesh/C18.452.648.189.875>
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p:direct-normalized/P699
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<http://purl.obolibrary.org/obo/DOID_DOID:9275>
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<http://wordnet-rdf.princeton.edu/rdf/id/14193379-n>
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wdt:P10283
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"C2781097277"
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wdt:P11143
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"Tyrosinemia"
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wdt:P1417
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"science/tyrosinemia"
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wdt:P1461
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"tyrosinaemia"
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wdt:P14914
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"D284818"
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wdt:P1550
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"284818"
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wdt:P1692
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"270.2"
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"C98640"
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wdt:P1995
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medical genetics
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wdt:P2293
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TYR
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HGD
|
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HPD
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TSPOAP1
|
|
TH
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TAT
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FAH
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wdt:P279
|
inborn disorder of phenylalanine or tyrosine metabolism
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wdt:P2888
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<http://identifiers.org/doid/DOID:9275>
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<http://purl.obolibrary.org/obo/DOID_9275>
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<http://www.orpha.net/ORDO/Orphanet_284818>
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|
wdt:P2892
|
"C0268483"
|
|
wdt:P31
|
type of disease
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|
wdt:P3827
|
"tyrosinemias"
|
|
wdt:P4229
|
"E70.2"
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|
"E70.21"
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|
wdt:P4527
|
"527790"
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wdt:P486
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"D020176"
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wdt:P492
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"276700"
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wdt:P493
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"270.2"
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|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0017307"
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|
wdt:P557
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"13478"
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|
"13486"
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|
"29836"
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|
wdt:P6366
|
"2781097277"
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wdt:P646
|
"/m/06hp_m"
|
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wdt:P665
|
"H00165"
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wdt:P672
|
"C10.228.140.163.100.875"
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|
"C16.320.565.100.880"
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|
"C16.320.565.189.875"
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|
"C18.452.132.100.875"
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|
"C18.452.648.100.880"
|
|
"C18.452.648.189.875"
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|
wdt:P673
|
"949816"
|
|
wdt:P699
|
"DOID:9275"
|
|
wdt:P7329
|
"5C50.1"
|
|
wdt:P7464
|
"tyrosinemia"
|
|
wdt:P7807
|
"1842978338"
|
|
wdt:P8814
|
"14193379-n"
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