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. 2017 Jun 11;2017:bax040. doi: 10.1093/database/bax040

Table 3.

JSON output example of the service S4 related to the generation of triplets for the annotation

{
  “gene”: “FGFR1”,
  “axis”: “Disease”,
  “publication”: “17154279”,
  “annotations”:
   [
  
  {
  
   “proposedRelation”:{“id”: “”, “name”: “causes disease”},
  
   “proposedObject”:{“id”: “C75479”, “name”: “Kallmann syndrome”},
  
   “proposedEco”:{“id”: “”, “name”: “”},
  
   “passage”:“In a new cohort of 141 unrelated patients affected by Kallmann syndrome we identified FGFR1 sequence variants in 17 patients, all in the heterozygous state.”
  
  },
  
  …
   ]
}

JSON output example of the service S4 related to the generation of triplets for the annotation. In this publication, PMID 17154279, the authors report on the possible implication of the gene FGFR1 in the Kallmann syndrome.