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- Ba6da578f4141c7f3edbb153f136fbe30 hasDbXref "Orphanet:213524" @default.
- Ba6da578f4141c7f3edbb153f136fbe30 hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- Ba6da578f4141c7f3edbb153f136fbe30 type Axiom @default.
- Ba6da578f4141c7f3edbb153f136fbe30 annotatedProperty IAO_0000115 @default.
- Ba6da578f4141c7f3edbb153f136fbe30 annotatedSource MONDO_0016249 @default.
- Ba6da578f4141c7f3edbb153f136fbe30 annotatedTarget "Ovarian cancer caused by germline mutations in various genes, usually associated with additional cancer risks. The most common are breast and ovarian cancer syndrome (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorectal cancer (HNPCC) due to mutations in DNA mismatch-repair genes. Mutations in STK11 gene, causing Peutz-Jeghers syndrome, are also associated with a risk of ovarian cancer (typically sex cord stromal tumors). Mutations in other genes, including RAD51C, RAD51D, PALB2, confer an elevated ovarian cancer risk in a minority of patients." @default.