{"@context":{"ns0":"http://www.ebi.ac.uk/efo/","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#","obo_purl":"http://purl.obolibrary.org/obo/","oboinowl_gen":"http://www.geneontology.org/formats/oboInOwl#","dc":"http://purl.org/dc/elements/1.1/","metadata_def":"http://data.bioontology.org/metadata/def/","metadata":"http://data.bioontology.org/metadata/"},"@graph":[{"@id":"ns0:EFO_0030063","@type":"owl:Class","rdfs:subClassOf":{"@id":"obo_purl:IAO_0000030"},"rdfs:label":"copy number assessment","rdfs:comment":"Assessment of the copy number of a genomic feature or region, referenced to the expected allele count in a given sample. Examples of an expected count would be: a) autosomal chromosome in human germline: 2; b) X-chromosome in human male: 1; c) triploid cancer cell line: 3, i.e. a region with 2 alleles in a triploid cell line would correspond to a low-level copy number loss.","obo_purl:IAO_0000115":"Result of genomic copy number assessment of a genomic element or region.","oboinowl_gen:hasExactSynonym":["copy number variation analysis","genomic copy number assessment"],"dc:creator":"paola","dc:date":{"@type":"http://www.w3.org/2001/XMLSchema#dateTime","@value":"2022-01-14T11:04:56Z"},"metadata:def/prefLabel":"copy number assessment","metadata:def/mappingLoom":"copynumberassessment","metadata:def/mappingSameURI":{"@id":"ns0:EFO_0030063"},"metadata:prefixIRI":"efo:EFO_0030063"},{"@id":"ns0:EFO_0030064","rdfs:subClassOf":{"@id":"ns0:EFO_0030063"}},{"@id":"ns0:EFO_0030066","rdfs:subClassOf":{"@id":"ns0:EFO_0030063"}}]}
{"@context":{"ns0":"http://www.ebi.ac.uk/efo/","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#","obo_purl":"http://purl.obolibrary.org/obo/","oboinowl_gen":"http://www.geneontology.org/formats/oboInOwl#","dc":"http://purl.org/dc/elements/1.1/","metadata_def":"http://data.bioontology.org/metadata/def/","metadata":"http://data.bioontology.org/metadata/"},"@graph":[{"@id":"ns0:EFO_0030063","@type":"owl:Class","rdfs:subClassOf":{"@id":"obo_purl:IAO_0000030"},"rdfs:label":"copy number assessment","rdfs:comment":"Assessment of the copy number of a genomic feature or region, referenced to the expected allele count in a given sample. Examples of an expected count would be: a) autosomal chromosome in human germline: 2; b) X-chromosome in human male: 1; c) triploid cancer cell line: 3, i.e. a region with 2 alleles in a triploid cell line would correspond to a low-level copy number loss.","obo_purl:IAO_0000115":"Result of genomic copy number assessment of a genomic element or region.","oboinowl_gen:hasExactSynonym":["copy number variation analysis","genomic copy number assessment"],"dc:creator":"paola","dc:date":{"@type":"http://www.w3.org/2001/XMLSchema#dateTime","@value":"2022-01-14T11:04:56Z"},"metadata:def/prefLabel":"copy number assessment","metadata:def/mappingLoom":"copynumberassessment","metadata:def/mappingSameURI":{"@id":"ns0:EFO_0030063"},"metadata:prefixIRI":"efo:EFO_0030063"},{"@id":"ns0:EFO_0030064","rdfs:subClassOf":{"@id":"ns0:EFO_0030063"}},{"@id":"ns0:EFO_0030066","rdfs:subClassOf":{"@id":"ns0:EFO_0030063"}}]}