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- NCIT_C17666 IAO_0000115 "Any mutation that appears in the gametes and which will therefore be transmitted to the progeny with some frequency." @default.
- NCIT_C17666 NCIT_A32 NCIT_C172272 @default.
- NCIT_C17666 NCIT_A32 NCIT_C177604 @default.
- NCIT_C17666 NCIT_NHC0 "C17666" @default.
- NCIT_C17666 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C17666 NCIT_P108 "Germline Variation" @default.
- NCIT_C17666 NCIT_P207 "C0206530" @default.
- NCIT_C17666 NCIT_P322 "CDISC" @default.
- NCIT_C17666 NCIT_P322 "GDC" @default.
- NCIT_C17666 NCIT_P325 "A gene change in the body's reproductive cells (egg or sperm) that becomes incorporated into the DNA of every cell in the body of offspring; germline mutations are passed on from parents to offspring." @default.
- NCIT_C17666 NCIT_P325 "Any inheritable variation in the DNA that is transmitted to the progeny with some frequency." @default.
- NCIT_C17666 NCIT_P366 "Germline_Mutation" @default.
- NCIT_C17666 NCIT_P375 "Germline" @default.
- NCIT_C17666 NCIT_P375 "Simple Germline Variation" @default.
- NCIT_C17666 normalizedInformationContent "71.519303452612405" @default.
- NCIT_C17666 referenceCount "74" @default.
- NCIT_C17666 hasExactSynonym "GERMLINE VARIATION" @default.
- NCIT_C17666 hasExactSynonym "Germline Mutation Abnormality" @default.
- NCIT_C17666 hasExactSynonym "Germline Mutation" @default.
- NCIT_C17666 hasExactSynonym "Germline Variant" @default.
- NCIT_C17666 hasExactSynonym "Germline Variation" @default.
- NCIT_C17666 hasExactSynonym "Hereditary Mutation" @default.
- NCIT_C17666 hasExactSynonym "Simple Germline Variation" @default.
- NCIT_C17666 hasExactSynonym "germline mutation" @default.
- NCIT_C17666 hasExactSynonym "hereditary mutation" @default.
- NCIT_C17666 inSubset NCIT_C157711 @default.
- NCIT_C17666 inSubset NCIT_C177537 @default.
- NCIT_C17666 inSubset NCIT_C181177 @default.
- NCIT_C17666 inSubset NCIT_C61410 @default.
- NCIT_C17666 inSubset NCIT_C66830 @default.
- NCIT_C17666 type Class @default.
- NCIT_C17666 isDefinedBy ncit.owl @default.
- NCIT_C17666 label "Germline Variation" @default.
- NCIT_C17666 subClassOf NCIT_C17666 @default.
- NCIT_C17666 subClassOf NCIT_C36391 @default.
- NCIT_C17666 subClassOf NCIT_C3910 @default.
- NCIT_C17666 subClassOf NCIT_C45576 @default.
- NCIT_C17666 subClassOf NCIT_C97926 @default.