wikipathways-collection

WikiPathways WP5169

• WikiPathways: WP5169 (classic)
• Species: Homo sapiens
• Scholia: WP5169

  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: 16
  • 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: 16

http://classic.wikipathways.org/instance/WP5169_r128214 "Lead poisoning" with graphId c929d
http://classic.wikipathways.org/instance/WP5169_r128214 "5-aminolevulinate dehydratase 
porphyria
" with graphId ee6da
http://classic.wikipathways.org/instance/WP5169_r128214 "Lead poisoning" with graphId d9fe0
http://classic.wikipathways.org/instance/WP5169_r128214 "Lead poisoning" with graphId e03fb
http://classic.wikipathways.org/instance/WP5169_r128214 "Erythropoietic protoporphyria
" with graphId b9cb4
http://classic.wikipathways.org/instance/WP5169_r128214 "Porphyria cutanea tarda

" with graphId c5f80
http://classic.wikipathways.org/instance/WP5169_r128214 "Hypertyrosinemia type I
" with graphId a2a0b
http://classic.wikipathways.org/instance/WP5169_r128214 "Variegate porphyria" with graphId c23b9
http://classic.wikipathways.org/instance/WP5169_r128214 "Hepatoerythropoietic porphyria" with graphId c2a46
http://classic.wikipathways.org/instance/WP5169_r128214 "Negative feedback" with graphId cd87e
http://classic.wikipathways.org/instance/WP5169_r128214 "Congenital erythropoietic porphyria" with graphId eeff0
http://classic.wikipathways.org/instance/WP5169_r128214 "Harderoporphyria" with graphId b1fc4
http://classic.wikipathways.org/instance/WP5169_r128214 "Hereditary coproporphyria
" with graphId d6d5e
http://classic.wikipathways.org/instance/WP5169_r128214 "Acute intermittent porphyria" with graphId f3658
http://classic.wikipathways.org/instance/WP5169_r128214 "X-linked sideroblastic anemia" with graphId b0352
http://classic.wikipathways.org/instance/WP5169_r128214 "X-linked protophyria" with graphId d6c81