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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C48287> ?p ?o ?g. }

• NCIT_C48287 IAO_0000115 "An autosomal dominant inherited syndrome characterized by the development of parathyroid adenoma or carcinoma, ossifying fibroma of the mandible and maxilla, renal neoplasms, and renal cysts." @default.
• NCIT_C48287 NCIT_A13 NCIT_C43569 @default.
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• NCIT_C48287 NCIT_P106 "Disease or Syndrome" @default.
• NCIT_C48287 NCIT_P108 "Hyperparathyroidism-Jaw Tumor Syndrome" @default.
• NCIT_C48287 NCIT_P207 "C1704981" @default.
• NCIT_C48287 NCIT_P322 "NICHD" @default.
• NCIT_C48287 NCIT_P325 "An autosomal dominant condition that may be associated with mutation(s) in the CDC73 gene, encoding cell division cycle protein 73 homolog. The condition is characterized by hyperfunctioning parathyroid adenomas and fibro-osseous tumors of the maxilla and mandible. This condition may also be associated with parathyroid carcinoma, Wilms tumor, and Hurthle cell thyroid adenomas." @default.
• NCIT_C48287 NCIT_P366 "Hyperparathyroidism-Jaw_Tumor_Syndrome" @default.
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