wikipathways-collection

WikiPathways WP4808

• WikiPathways: WP4808 (classic)
• Species: Homo sapiens
• Scholia: WP4808

  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: 18
  • 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 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: 1

Fails

InteractionTests.interactionsWithLabels

Interactions found that involve Labels: 18

http://classic.wikipathways.org/instance/WP4808_r128905 "Hypertrophy" with graphId b7a
http://classic.wikipathways.org/instance/WP4808_r128905 "WNT signaling
canonical / non-canonical" with graphId bed
http://classic.wikipathways.org/instance/WP4808_r128905 "Proliferation" with graphId d5f
http://classic.wikipathways.org/instance/WP4808_r128905 "BMPs" with graphId b2d
http://classic.wikipathways.org/instance/WP4808_r128905 "Mineralization" with graphId e4d
http://classic.wikipathways.org/instance/WP4808_r128905 "Dying" with graphId b59
http://classic.wikipathways.org/instance/WP4808_r128905 "Full differentiation" with graphId fba0c
http://classic.wikipathways.org/instance/WP4808_r128905 "Integrins" with graphId d3b0f
http://classic.wikipathways.org/instance/WP4808_r128905 "Vascular invasion" with graphId e31d0
http://classic.wikipathways.org/instance/WP4808_r128905 "Gs" with graphId fc068
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:600430
Chromosome 2q37 deletion syndrome" with graphId f8e71
http://classic.wikipathways.org/instance/WP4808_r128905 "Osteoblastic
differentiation" with graphId f20
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:613073
Metaphyseal anadysplasia 2" with graphId e6bf2
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:156500
Metaphyseal chondrodysplasia, Schmid type" with graphId f4641
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:245150
Keutel syndrome" with graphId c0def
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:614732
Intrauterine growth retardation, metaphyseal dysplasia, 
adrenal hypoplasia congenita, and genital anomalies" with graphId f99f8
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:271665
Spondylometaepiphyseal dysplasia, short limb-hand type" with graphId b7cc5
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:613848
Osteogenesis imperfecta, type X" with graphId aa6b4