{"@context":{"obo_purl":"http://purl.obolibrary.org/obo/","rdf":"http://www.w3.org/1999/02/22-rdf-syntax-ns#","owl":"http://www.w3.org/2002/07/owl#","rdfs":"http://www.w3.org/2000/01/rdf-schema#","skos":"http://www.w3.org/2004/02/skos/core#","oboinowl_gen":"http://www.geneontology.org/formats/oboInOwl#","ns0":"http://purl.oboInOwllibrary.org/oboInOwl/chebi#","ns1":"http://purl.obolibrary.org/obo/chebi#","metadata_def":"http://data.bioontology.org/metadata/def/"},"@graph":[{"@id":"obo_purl:CHEBI_26004","@type":"owl:Class","rdfs:subClassOf":{"@id":"obo_purl:CHEBI_26848"},"rdfs:label":["phenylpropanoid",{"@type":"http://www.w3.org/XML/1998/namespacestring","@value":"phenylpropanoid"}],"skos:notation":"CHEBI:26004","obo_purl:IAO_0000115":"Any organic aromatic compound with a structure based on a phenylpropane skeleton. The class includes naturally occurring phenylpropanoid esters, flavonoids, anthocyanins, coumarins and many small phenolic molecules as well as their semi-synthetic and synthetic analogues. Phenylpropanoids are also precursors of lignin.","obo_purl:IAO_0000412":{"@id":"obo_purl:cdno.owl"},"oboinowl_gen:hasDbXref":"Wikipedia:Phenylpropanoid","oboinowl_gen:hasOBONamespace":"chebi_ontology","oboinowl_gen:id":"CHEBI:26004","oboinowl_gen:inSubset":[{"@id":"ns0:3_STAR"},{"@id":"ns1:3_STAR"}],"metadata_def:prefLabel":"phenylpropanoid","oboinowl_gen:hasRelatedSynonym":"phenylpropanoids","metadata_def:mappingLoom":"phenylpropanoid","metadata_def:mappingSameURI":{"@id":"obo_purl:CHEBI_26004"}},{"@id":"obo_purl:CHEBI_4917","rdfs:subClassOf":{"@id":"obo_purl:CHEBI_26004"}},{"@id":"obo_purl:CHEBI_25036","rdfs:subClassOf":{"@id":"obo_purl:CHEBI_26004"}},{"@id":"obo_purl:CHEBI_23403","rdfs:subClassOf":{"@id":"obo_purl:CHEBI_26004"}},{"@id":"obo_purl:CHEBI_4918","rdfs:subClassOf":{"@id":"obo_purl:CHEBI_26004"}},{"@id":"obo_purl:ECTO_9000345","obo_purl:RO_0002309":{"@id":"obo_purl:CHEBI_26004"}}]}