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- NCIT_C125386 IAO_0000115 "A very rare, autosomal recessive inherited condition caused by mutations in the SCN9A gene. It is characterized by a lack of the ability to perceive physical pain." @default.
- NCIT_C125386 NCIT_NHC0 "C125386" @default.
- NCIT_C125386 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C125386 NCIT_P108 "Indifference to Pain, Congenital, Autosomal Recessive" @default.
- NCIT_C125386 NCIT_P207 "C0002768" @default.
- NCIT_C125386 NCIT_R176 NCIT_C114810 @default.
- NCIT_C125386 NCIT_R176 NCIT_C16612 @default.
- NCIT_C125386 NCIT_R176 NCIT_C21295 @default.
- NCIT_C125386 NCIT_R176 NCIT_C25869 @default.
- NCIT_C125386 NCIT_R176 NCIT_C25993 @default.
- NCIT_C125386 NCIT_R176 NCIT_C26039 @default.
- NCIT_C125386 NCIT_R176 NCIT_C28533 @default.
- NCIT_C125386 normalizedInformationContent "100" @default.
- NCIT_C125386 referenceCount "1" @default.
- NCIT_C125386 hasExactSynonym "CIP" @default.
- NCIT_C125386 hasExactSynonym "Congenital Insensitivity to Pain" @default.
- NCIT_C125386 hasExactSynonym "Congenital Pain Insensitivity" @default.
- NCIT_C125386 hasExactSynonym "Indifference to Pain, Congenital, Autosomal Recessive" @default.
- NCIT_C125386 type Class @default.
- NCIT_C125386 isDefinedBy ncit.owl @default.
- NCIT_C125386 label "Indifference to Pain, Congenital, Autosomal Recessive" @default.
- NCIT_C125386 subClassOf B222f8f1202192d26d22457a8cb855fa9 @default.
- NCIT_C125386 subClassOf B3a5d61a89837bdf61a6bdbb0545e1299 @default.
- NCIT_C125386 subClassOf NCIT_C125386 @default.
- NCIT_C125386 subClassOf NCIT_C2991 @default.
- NCIT_C125386 subClassOf NCIT_C4873 @default.
- NCIT_C125386 subClassOf NCIT_C53529 @default.
- NCIT_C125386 subClassOf NCIT_C53543 @default.
- NCIT_C125386 subClassOf NCIT_C53547 @default.
- NCIT_C125386 subClassOf NCIT_C7057 @default.