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- NCIT_C192671 IAO_0000115 "A hereditary neoplastic syndrome characterized by germline mutations of homologous recombination (HR) pathway genes. It is associated with an increased risk of developing various malignancies including breast, ovarian, pancreatic, and prostate carcinoma, and melanoma." @default.
- NCIT_C192671 NCIT_NHC0 "C192671" @default.
- NCIT_C192671 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C192671 NCIT_P108 "Hereditary Tumor Syndrome Associated with Homologous Recombination Pathway Mutations" @default.
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- NCIT_C192671 hasExactSynonym "Hereditary Homologous Recombination Cancer Syndrome" @default.
- NCIT_C192671 hasExactSynonym "Hereditary Tumor Syndrome Associated with Homologous Recombination Pathway Mutations" @default.
- NCIT_C192671 type Class @default.
- NCIT_C192671 isDefinedBy ncit.owl @default.
- NCIT_C192671 label "Hereditary Tumor Syndrome Associated with Homologous Recombination Pathway Mutations" @default.
- NCIT_C192671 subClassOf NCIT_C192671 @default.
- NCIT_C192671 subClassOf NCIT_C28193 @default.
- NCIT_C192671 subClassOf NCIT_C2991 @default.
- NCIT_C192671 subClassOf NCIT_C3101 @default.
- NCIT_C192671 subClassOf NCIT_C3266 @default.
- NCIT_C192671 subClassOf NCIT_C54705 @default.
- NCIT_C192671 subClassOf NCIT_C7057 @default.
- NCIT_C192671 equivalentClass Bb70dda4fb85e65f51401fbce410b4816 @default.
- NCIT_C192671 equivalentClass Bfb6dc427c420da743b4431171a31dae8 @default.