PropertyValue
?:definition
  • Molecular assay reagents intended to identify mutations in the potassium voltage-gated channel, KQT-like subfamily, member 1 (KCNQ1) gene, located at chromosome 11p15.5, which encodes for a protein involved in potassium-channel formation and function and helps move potassium out of the cell. Mutations at this locus have been identified in patients with familial atrial fibrillation, JLNS, Romano-Ward syndrome, and short QT syndromes.
?: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/C3689749_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/C3689749_UMD>
<http://purl.org/net/provenance/ns#createdBy>
Anon_1   (more)
expand all