PropertyValue
?:definition
  • A relatively rare syndrome of diploidy (the state of having two full sets of homologous chromosomes) associated with triploidy (the presence of three haploid sets of chromosomes) together with mental and growth retardation, facial and body asymmetry, malformed and apparently low-set ears, and syndactyly.
?:hasCUIAnnotation
?:hasGeneratedBy
?:type

Metadata

Anon_0  
<http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://purl.org/net/provenance/ns#DataItem>
<http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.w3.org/2004/03/trix/rdfg-1/Graph>
<http://xmlns.com/foaf/0.1/primaryTopic> <https://research.tib.eu/covid-19/entity/C0795883_JABL>
<http://xmlns.com/foaf/0.1/topic> Anon_0
<http://www.ontologydesignpatterns.org/cp/owl/informationrealization.owl#realizes> <https://research.tib.eu/covid-19/data/entity/C0795883_JABL>
<http://purl.org/net/provenance/ns#createdBy>
Anon_1   (more)
expand all