{"code":"C188690","name":"Variant Calling","terminology":"ncit","version":"26.09d","conceptStatus":"DEFAULT","leaf":true,"active":true,"synonyms":[{"name":"Variant calling","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"FDA","subSource":"pFDA"},{"name":"Variant Calling","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Variant Calling","type":"Preferred_Name","typeCode":"P108"}],"definitions":[{"definition":"Technology that detects differences between an individual's DNA sequence and a reference DNA sequence.","code":"P97","type":"DEFINITION","source":"NCI"}],"properties":[{"code":"P322","type":"Contributing_Source","value":"FDA"},{"code":"P208","type":"NCI_META_CUI","value":"CL1793769"},{"code":"P106","type":"Semantic_Type","value":"Intellectual Product"}]}