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- NCIT_C129303 IAO_0000115 "An autosomal recessive disorder that is associated with mutation(s) in the CFTR gene, encoding cystic fibrosis transmembrane conductance regulator. Mutation(s) in the same gene are associated with cystic fibrosis." @default.
- NCIT_C129303 NCIT_NHC0 "C129303" @default.
- NCIT_C129303 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C129303 NCIT_P108 "Congenital Bilateral Aplasia of the Vas Deferens" @default.
- NCIT_C129303 NCIT_P207 "C0403814" @default.
- NCIT_C129303 NCIT_P322 "Cellosaurus" @default.
- NCIT_C129303 NCIT_R176 NCIT_C111925 @default.
- NCIT_C129303 NCIT_R176 NCIT_C16612 @default.
- NCIT_C129303 NCIT_R176 NCIT_C21281 @default.
- NCIT_C129303 NCIT_R176 NCIT_C21295 @default.
- NCIT_C129303 NCIT_R176 NCIT_C25941 @default.
- NCIT_C129303 NCIT_R176 NCIT_C28533 @default.
- NCIT_C129303 normalizedInformationContent "100" @default.
- NCIT_C129303 referenceCount "1" @default.
- NCIT_C129303 hasExactSynonym "CAVD" @default.
- NCIT_C129303 hasExactSynonym "Congenital Bilateral Aplasia of the Vas Deferens" @default.
- NCIT_C129303 inSubset NCIT_C165258 @default.
- NCIT_C129303 inSubset NCIT_C192842 @default.
- NCIT_C129303 type Class @default.
- NCIT_C129303 isDefinedBy ncit.owl @default.
- NCIT_C129303 label "Congenital Bilateral Aplasia of the Vas Deferens" @default.
- NCIT_C129303 subClassOf B0d697f07bdd8e5d1a4e2daef773251a1 @default.
- NCIT_C129303 subClassOf Be3d0f703e3fcc49135b598d93a00a638 @default.
- NCIT_C129303 subClassOf NCIT_C129303 @default.
- NCIT_C129303 subClassOf NCIT_C2991 @default.
- NCIT_C129303 subClassOf NCIT_C4873 @default.
- NCIT_C129303 subClassOf NCIT_C53529 @default.
- NCIT_C129303 subClassOf NCIT_C53543 @default.
- NCIT_C129303 subClassOf NCIT_C53547 @default.
- NCIT_C129303 subClassOf NCIT_C7057 @default.