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- NCIT_C171071 IAO_0000115 "A change in the nucleotide sequence of the BAP1 gene that is associated with increased risk of disease." @default.
- NCIT_C171071 NCIT_NHC0 "C171071" @default.
- NCIT_C171071 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C171071 NCIT_P107 "Deleterious BAP1 Gene Mutation" @default.
- NCIT_C171071 NCIT_P108 "Deleterious BAP1 Gene Mutation" @default.
- NCIT_C171071 NCIT_P208 "CL1405449" @default.
- NCIT_C171071 NCIT_P322 "CTRP" @default.
- NCIT_C171071 NCIT_R177 NCIT_C16612 @default.
- NCIT_C171071 NCIT_R177 NCIT_C20766 @default.
- NCIT_C171071 NCIT_R177 NCIT_C21281 @default.
- NCIT_C171071 NCIT_R177 NCIT_C25804 @default.
- NCIT_C171071 NCIT_R177 NCIT_C26003 @default.
- NCIT_C171071 NCIT_R177 NCIT_C28404 @default.
- NCIT_C171071 normalizedInformationContent "100" @default.
- NCIT_C171071 referenceCount "1" @default.
- NCIT_C171071 hasExactSynonym "Deleterious BAP1 Gene Mutation" @default.
- NCIT_C171071 hasExactSynonym "Deleterious BAP1 Mutation" @default.
- NCIT_C171071 hasExactSynonym "Deleterious BRCA1 Associated Protein 1 Gene Mutation" @default.
- NCIT_C171071 hasExactSynonym "Deleterious BRCA1-Associated Protein 1 Gene Mutation" @default.
- NCIT_C171071 hasExactSynonym "Deleterious UCHL2 Gene Mutation" @default.
- NCIT_C171071 inSubset NCIT_C116977 @default.
- NCIT_C171071 inSubset NCIT_C142799 @default.
- NCIT_C171071 inSubset NCIT_C142800 @default.
- NCIT_C171071 type Class @default.
- NCIT_C171071 isDefinedBy ncit.owl @default.
- NCIT_C171071 label "Deleterious BAP1 Gene Mutation" @default.
- NCIT_C171071 subClassOf NCIT_C128813 @default.
- NCIT_C171071 subClassOf NCIT_C171071 @default.
- NCIT_C171071 subClassOf NCIT_C36391 @default.
- NCIT_C171071 subClassOf NCIT_C3910 @default.
- NCIT_C171071 subClassOf NCIT_C45576 @default.
- NCIT_C171071 subClassOf NCIT_C93102 @default.
- NCIT_C171071 subClassOf NCIT_C97926 @default.
- NCIT_C171071 subClassOf NCIT_C97927 @default.