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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C3076> ?p ?o ?g. }

• NCIT_C3076 IAO_0000115 "An autosomal dominant hereditary syndrome characterized by a variety of hamartomas and neoplasms including verrucous skin lesions, fibromas of the oral cavity, facial trichilemmomas, hamartomatous colonic polyps, thyroid neoplasms, breast cancer, and dysplastic gangliocytomas of the cerebellum." @default.
• NCIT_C3076 NCIT_A13 NCIT_C18256 @default.
• NCIT_C3076 NCIT_A32 NCIT_C17103 @default.
• NCIT_C3076 NCIT_NHC0 "C3076" @default.
• NCIT_C3076 NCIT_P106 "Disease or Syndrome" @default.
• NCIT_C3076 NCIT_P107 "Cowden Syndrome" @default.
• NCIT_C3076 NCIT_P108 "Cowden Syndrome" @default.
• NCIT_C3076 NCIT_P207 "C0018553" @default.
• NCIT_C3076 NCIT_P322 "CCPS" @default.
• NCIT_C3076 NCIT_P322 "CTRP" @default.
• NCIT_C3076 NCIT_P322 "Cellosaurus" @default.
• NCIT_C3076 NCIT_P322 "GDC" @default.
• NCIT_C3076 NCIT_P325 "An inherited disorder marked by the formation of many noncancerous growths called hamartomas. These growths occur in the skin, breast, thyroid, colon, intestines, and inside of the mouth. Patients with Cowden syndrome are at increased risk of certain types of cancer, including breast and thyroid." @default.
• NCIT_C3076 NCIT_P366 "Cowden_Syndrome" @default.
• NCIT_C3076 NCIT_P375 "Cowden Syndrome" @default.
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