wikipathways-collection

WikiPathways WP5173

• WikiPathways: WP5173 (classic)
• Species: Homo sapiens
• Scholia: WP5173

  Tests

• CASMetabolitesTests: all 2 tests OK!
• ChEBIMetabolitesTests: all 5 tests OK!
• ChemSpiderTests: all 2 tests OK!
• DataNodesTests: all 5 tests OK!
• EnsemblTests: all 4 tests OK!
• GeneTests: all 4 tests OK!
• GeneralTests: all 15 tests OK!
• HMDBSecMetabolitesTests: all 3 tests OK!
• InteractionTests
  • noMetaboliteToNonMetaboliteConversions: .. all OK!
  • noNonMetaboliteToMetaboliteConversions: .. all OK!
  • noGeneProteinConversions: .. all OK!
  • nonNumericIDs: .. all OK!
  • interactionsWithLabels: .x we found 1 problem(s):
    • Interactions found that involve Labels: 13
  • possibleTranslocations: .. all OK!
  • noProteinProteinConversions: .. all OK!
  • incorrectKEGGIdentifiers: .. all OK!
• KEGGMetaboliteTests: all 2 tests OK!
• LIPIDMAPSTests: all 1 tests OK!
• MetaboliteStructureTests: all 1 tests OK!
• MetabolitesTests: all 14 tests OK!
• OudatedDataSourcesTests: all 24 tests OK!
• PathwayTests: all 7 tests OK!
• ProteinsTests: all 2 tests OK!
• PubChemMetabolitesTests: all 3 tests OK!
• ReferencesTests: all 6 tests OK!
• UniProtTests: all 5 tests OK!
• WikidataTests: all 4 tests OK!

Summary

• Number of test classes: 20
• Number of tests: 117
• Number of assertions: 235
• Number of fails: 1

Fails

InteractionTests.interactionsWithLabels

Interactions found that involve Labels: 13

http://classic.wikipathways.org/instance/WP5173_r136172 "Fanconi-Bickel syndrome" with graphId fd3d0
http://classic.wikipathways.org/instance/WP5173_r136172 "Uridine diphosphate 
galactose-4-epimerase 
deficiency" with graphId c9ff6
http://classic.wikipathways.org/instance/WP5173_r136172 "Congenital disorder of glycosylation, 
type It" with graphId de139
http://classic.wikipathways.org/instance/WP5173_r136172 "Glycogen storage 
disease IV" with graphId aaa50
http://classic.wikipathways.org/instance/WP5173_r136172 "Glycogen storage disease 0, muscle" with graphId fbaa3
http://classic.wikipathways.org/instance/WP5173_r136172 "Glycogen storage disease XV" with graphId abc2c
http://classic.wikipathways.org/instance/WP5173_r136172 "Galactosaemia" with graphId a8706
http://classic.wikipathways.org/instance/WP5173_r136172 "Intestinal glucose-galactose 
malabsorption" with graphId d61c1
http://classic.wikipathways.org/instance/WP5173_r136172 "Polyglucosan body myopathy 2" with graphId b5440
http://classic.wikipathways.org/instance/WP5173_r136172 "Glycogen storage 
disease VI" with graphId ae5e6
http://classic.wikipathways.org/instance/WP5173_r136172 "Galactokinase deficiency" with graphId d2625
http://classic.wikipathways.org/instance/WP5173_r136172 "Glycogen storage disease 0, liver" with graphId f124e
http://classic.wikipathways.org/instance/WP5173_r136172 "Polyglucosan body neuropathy" with graphId eba21