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- B98ffc8d03fc5149d2760d0c7630e0e6f NCIT_P378 "NCI" @default.
- B98ffc8d03fc5149d2760d0c7630e0e6f type Axiom @default.
- B98ffc8d03fc5149d2760d0c7630e0e6f annotatedProperty IAO_0000115 @default.
- B98ffc8d03fc5149d2760d0c7630e0e6f annotatedSource NCIT_C52076 @default.
- B98ffc8d03fc5149d2760d0c7630e0e6f annotatedTarget "Human HMGB1 wild-type allele is located within 13q12 and is approximately 159 kb in length. This allele, which encodes high mobility group protein B1, is involved in a number of DNA-related subcellular processes such as initiation of transcription, DNA repair and DNA recombination. Expression of the HMGB1 gene is associated with inflammation resulting in both lethal conditions (e.g., endotoxemia, sepsis) and diseases such as arthritis." @default.