PropertyValue
?:definition
  • Molecular assay reagents intended to identify mutations in the patched homologue (PTCH) gene, located at chromosome 9q22.3, which encodes for a protein implicated in the formation of embryonic structures and in tumorigenesis and that functions as a tumor suppressor. This genetic mutation has been identified in patients with holoprosencephaly-7 and nevoid basal cell carcinoma syndrome (NBCSS), also known as Gorlin\'s syndrome.
?: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/C3689641_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/C3689641_UMD>
<http://purl.org/net/provenance/ns#createdBy>
Anon_1   (more)
expand all