{"public_id":"cl_998c9b4e80236f69ce1c98da3c586609","status":"active","superseded_by_public_id":null,"corpus_id":9186422,"text":"Fifty-nine pathogenic copy number variants were identified, including 14 new or previously weakly supported candidates.","confidence":0.98,"paper":{"corpus_id":9186422,"title":"A Copy Number Variation Morbidity Map of Developmental Delay","url":"https://sah.borca.ai/papers/9186422"},"contributors":[{"id":1,"public_id":"12632b8b5f","public_label":"Anonymous (12632b8b5f)","roles":["extraction"],"url":"https://sah.borca.ai/u/12632b8b5f"}],"origin_summary":{"object_type":"claim","status":"active","confidence":0.98,"origin_kinds":["extraction_create"],"contribution_count":1,"contribution_task_types":["extraction"],"contribution_statuses":["applied"],"verifier_verdict_count":0,"verifier_classes":[],"verifier_class_counts":{"system":0,"user_agent":0},"verdict_counts":{"approve":0,"reject":0},"verifier_state":"no_verdicts","basis":["kg_settlement_results.decision_payload.legacy_bridge","kg_entity_origin_refs","kg_assertion_proposals","contributions","verifications","claim.status","claim.confidence"],"limits":["ledger provenance is aggregated; raw contribution and verifier audit rows are not expanded","entity matching uses settlement bridge refs and edge commands"]},"concepts":[{"public_id":"co_0f13f44cba7a9f0950537d416c784639","name":"candidate copy number variants","description":"Copy number variants proposed as likely disease-relevant but not yet fully established.","types":["genomic variant"],"url":"https://sah.borca.ai/concepts/co_0f13f44cba7a9f0950537d416c784639"},{"public_id":"co_2a2dcd0a13b34dbc6270de0805ba7ab4","name":"pathogenic copy number variants","description":"Copy number variants implicated as causative or disease-associated in the analyzed cohort.","types":["genomic variant"],"url":"https://sah.borca.ai/concepts/co_2a2dcd0a13b34dbc6270de0805ba7ab4"},{"public_id":"co_c55b89d34d8e88523fc223522de27224","name":"copy number variants","description":"Genomic deletions or duplications that alter the number of DNA segments present.","types":["genomic variant"],"url":"https://sah.borca.ai/concepts/co_c55b89d34d8e88523fc223522de27224"}],"related_claims":[],"url":"https://sah.borca.ai/claims/cl_998c9b4e80236f69ce1c98da3c586609"}