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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C128801> ?p ?o ?g. }

Showing items 1 to 100 of ±133 with 100 items per page.

NCIT_C128801 IAO_0000115 "An autosomal dominant genetic disorder caused by mutations in the CDKN2A gene, encoding cyclin-dependent kinase inhibitor 2A. The condition is characterized by cutaneous malignant melanoma associated with this genetic alteration." @default.
NCIT_C128801 NCIT_A13 NCIT_C18022 @default.
NCIT_C128801 NCIT_NHC0 "C128801" @default.
NCIT_C128801 NCIT_P106 "Neoplastic Process" @default.
NCIT_C128801 NCIT_P108 "Cutaneous Malignant Melanoma 2" @default.
NCIT_C128801 NCIT_P207 "C1835044" @default.
NCIT_C128801 NCIT_P322 "Cellosaurus" @default.
NCIT_C128801 NCIT_P363 "Malignant" @default.
NCIT_C128801 NCIT_R100 NCIT_C12219 @default.
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