wikipathways-collection

WikiPathways WP5190

• WikiPathways: WP5190 (classic)
• Species: Homo sapiens
• Scholia: WP5190

  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 13 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: 6
  • possibleTranslocations: .x we found 1 problem(s):
    • Interactions between identical nodes: 2
  • 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 8 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: 99
• Number of assertions: 200
• Number of fails: 2

Fails

InteractionTests.interactionsWithLabels

Interactions found that involve Labels: 6

http://classic.wikipathways.org/instance/WP5190_r128231 "Creatine
transporter
deficiency" with graphId ed29a
http://classic.wikipathways.org/instance/WP5190_r128231 "Ornithine 
aminotransferase 
deficiency" with graphId b9a19
http://classic.wikipathways.org/instance/WP5190_r128231 "Gyrate atrophy 
of choroid 
and retina" with graphId ebf2e
http://classic.wikipathways.org/instance/WP5190_r128231 "Guanidinoacetate 
methyltransferase 
deficiency" with graphId cdd76
http://classic.wikipathways.org/instance/WP5190_r128231 "Arginine/glycine
amidinotransferase
deficiency" with graphId b885b
http://classic.wikipathways.org/instance/WP5190_r128231 "Fanconi 
renotubular 
syndrome 1" with graphId b63a7

Possible MIM translocation

Interactions between identical nodes: 2

http://classic.wikipathways.org/instance/WP5190_r128231 http://rdf.wikipathways.org/Pathway/WP5190_r128231/WP/Interaction/id56c64cc3 "Creatinine" (https://identifiers.org/chebi/CHEBI:16737) and 
Creatinine" (https://identifiers.org/chebi/CHEBI:16737)
http://classic.wikipathways.org/instance/WP5190_r128231 http://rdf.wikipathways.org/Pathway/WP5190_r128231/WP/Interaction/id1dd22822 "Creatine" (https://identifiers.org/chebi/CHEBI:16919) and 
Creatine" (https://identifiers.org/chebi/CHEBI:16919)

More details at https://www.wikipathways.org/WikiPathwaysCurator/InteractionTests/possibleTranslocations