PropertyValue
?:definition
  • Molecular assay reagents intended to identify deletions or duplications of the epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) (EPM2A) gene, located at chromosome 6q24, which encodes the protein laforin. Genetic variants at this locus have been associated with Lafora disease.
?: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/C4053102_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/C4053102_UMD>
<http://purl.org/net/provenance/ns#createdBy>
Anon_1   (more)
expand all