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- NCIT_C120106 IAO_0000115 "Insufficient circulating insulin-like growth factor-I." @default.
- NCIT_C120106 NCIT_A13 NCIT_C24485 @default.
- NCIT_C120106 NCIT_NHC0 "C120106" @default.
- NCIT_C120106 NCIT_P106 "Finding" @default.
- NCIT_C120106 NCIT_P108 "Insulin Growth Factor I Deficiency" @default.
- NCIT_C120106 NCIT_P207 "C1837475" @default.
- NCIT_C120106 NCIT_P322 "NICHD" @default.
- NCIT_C120106 NCIT_P325 "Growth hormone insensitivity/resistance caused by loss-of-function mutation(s) in the IGF1 gene, encoding insulin-like growth factor I (IGF-I). This condition is characterized by severe prenatal and/or postnatal growth failure, sensorineural deafness, neurocognitive deficiencies, and elevated GH concentrations accompanied by low IGF-I concentrations." @default.
- NCIT_C120106 normalizedInformationContent "100" @default.
- NCIT_C120106 referenceCount "1" @default.
- NCIT_C120106 hasExactSynonym "IGF-I Deficiency" @default.
- NCIT_C120106 hasExactSynonym "IGF1 Deficiency" @default.
- NCIT_C120106 hasExactSynonym "Insulin Growth Factor I Deficiency" @default.
- NCIT_C120106 hasExactSynonym "Insulin-like Growth Factor I Deficiency" @default.
- NCIT_C120106 inSubset NCIT_C118467 @default.
- NCIT_C120106 inSubset NCIT_C90259 @default.
- NCIT_C120106 type Class @default.
- NCIT_C120106 isDefinedBy ncit.owl @default.
- NCIT_C120106 label "Insulin Growth Factor I Deficiency" @default.
- NCIT_C120106 subClassOf NCIT_C120106 @default.
- NCIT_C120106 subClassOf NCIT_C3367 @default.
- NCIT_C120106 subClassOf NCIT_C36278 @default.
- NCIT_C120106 subClassOf NCIT_C36285 @default.
- NCIT_C120106 subClassOf NCIT_C7057 @default.
- NCIT_C120106 subClassOf NCIT_C92809 @default.