This HTML5 document contains 41 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

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Statements

Subject Item
wd:Q27674935
rdf:type
wikibase:Item
schema:description
Krankheit مرض يصيب الإنسان hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYOZ2 gene on chromosome 4q26 хвороба
p:P2888
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n11:0110322 n12:DOID_0110322
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n5:0110322
wdt:P5270
MONDO_0013455
wdt:P699
DOID:0110322
rdfs:label
hypertrophic cardiomyopathy 16
skos:prefLabel
hypertrophic cardiomyopathy 16
schema:name
hypertrophic cardiomyopathy 16
p:P31
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wdt:P31
wd:Q112193867
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wdt:P11430
DI-03037
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155
wdt:P2293
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613838
skos:altLabel
cardiomyopathy familial hypertrophic 16 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; CMH16 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16 Cardiomyopathy, Familial Hypertrophic, type 16 CMH16 hypertrophic cardiomyopathy type 16
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C3151204
wdt:P5008
wd:Q4099686