{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":5,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:9884","source":"HGNC:9884|RB transcriptional corepressor 1","targets":["GENCC_000101-HGNC_9884-MONDO_0005105-HP_0000006-GENCC_100003|RB1|melanoma|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_9884-OMIM_180200-HP_0000006-GENCC_100001|RB1|hereditary retinoblastoma|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000106-HGNC_9884-OMIM_180200-HP_0000006-GENCC_100002|RB1|hereditary retinoblastoma|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_9884-ORPHANET_357027-HP_0000006-GENCC_100009|RB1|hereditary retinoblastoma|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_9884-OMIM_180200-HP_0000006-GENCC_100001|RB1|hereditary retinoblastoma|Definitive|Autosomal dominant|G2P"]}]}