PropertyValue
?:definition
  • Molecular assay reagents intended to identify mutations in the amyloid beta (A4) precursor protein (protease nexin-II) (APP) gene, located at chromosome 21q21, which functions as a cell surface receptor and performs physiologic functions on the surface of neurons. Mutations at this locus have been identified in patients with familial (early onset) Alzheimer\'s disease (AD) type 1, Flemish-type AD, and cerebral hemorrhage with amyloidosis (HCHWAD).
?: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/C3689915_UMD>
<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/C3689915_UMD>
<http://purl.org/net/provenance/ns#createdBy>
Anon_1   (more)
expand all