PropertyValue
?:definition
  • A chromosomal abnormality consisting of the presence of part or all of a third copy of chromosome 21 in somatic cells.
?:hasCUIAnnotation
?:hasGeneratedBy
?:type

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<http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.w3.org/2004/03/trix/rdfg-1/Graph>
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