{
  "dbId" : 5632968,
  "stId" : "R-HSA-5632968",
  "speciesName" : "Homo sapiens",
  "nodes" : [ {
    "dbId" : 5357525,
    "stId" : "R-HSA-5357525",
    "displayName" : "MSH2 [nucleoplasm]",
    "schemaClass" : "EntityWithAccessionedSequence",
    "speciesId" : 48887,
    "diagramIds" : [ 112, 253 ],
    "identifier" : "P43246",
    "standardIdentifier" : "uniprot:P43246",
    "referenceType" : "ReferenceGeneProduct",
    "geneNames" : [ "MSH2" ],
    "parents" : [ ],
    "children" : [ ]
  }, {
    "dbId" : 5632954,
    "stId" : "R-HSA-5632954",
    "displayName" : "MSH6 L222* [nucleoplasm]",
    "schemaClass" : "EntityWithAccessionedSequence",
    "speciesId" : 48887,
    "diagramIds" : [ 150338 ],
    "identifier" : "P52701",
    "standardIdentifier" : "uniprot:P52701",
    "referenceType" : "ReferenceGeneProduct",
    "geneNames" : [ "MSH6", "GTBP" ],
    "parents" : [ ],
    "children" : [ ]
  } ],
  "edges" : [ {
    "dbId" : 5632970,
    "stId" : "R-HSA-5632970",
    "displayName" : "MSH6 variant:MSH2-defective DNA mismatch repair",
    "schemaClass" : "FailedReaction",
    "speciesId" : 0,
    "inputs" : [ 5632954, 5357525 ],
    "efs" : [ 5632954 ],
    "diagramIds" : [ 150337 ],
    "entityFunctionalStatus" : [ 5632954 ]
  } ]
}