PropertyValue
?:definition
  • Molecular assay reagents intended to identify mutations in genes associated with Alport syndrome, a heritable disorder affecting kidney function as well as hearing loss and abnormalities of the eyes. Genetic variants at multiple loci have been associated with Alport syndrome. These reagents are intended to detect mutations in multiple Alport syndrome-associated loci simultaneously.
?: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/C4286177_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/C4286177_UMD>
<http://purl.org/net/provenance/ns#createdBy>
Anon_1   (more)
expand all