{"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:7989","source":"HGNC:7989|NRAS proto-oncogene, GTPase","targets":["GENCC_000104-HGNC_7989-MONDO_0015280-HP_0000006-GENCC_100002|NRAS|cardiofaciocutaneous syndrome|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_7989-OMIM_613224-HP_0000006-GENCC_100002|NRAS|Noonan syndrome 6|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_7989-OMIM_613224-HP_0000006-GENCC_100002|NRAS|Noonan syndrome 6|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_7989-ORPHANET_648-HP_0000006-GENCC_100009|NRAS|Noonan syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_7989-OMIM_613224-HP_0000006-GENCC_100001|NRAS|Noonan syndrome 6|Definitive|Autosomal dominant|G2P"]}]}