imd-pathway-curation

WikiPathways WP5173

Tests

Summary

Fails

IEMPathwayTests.allMetabolitesInteract

Found metabolites without interaction: 3

https://identifiers.org/wikipathways/WP5173 has an metabolite not linked to an interaction: UDP-galactose
https://identifiers.org/wikipathways/WP5173 has an metabolite not linked to an interaction: Glycogen
https://identifiers.org/wikipathways/WP5173 has an metabolite not linked to an interaction: Glucose-6-phosphate

IEMPathwayTests.metabolicConversionIdentifiersCommon

Unexpected data source for the metabolic conversion: 1

https://identifiers.org/wikipathways/WP5173 http://rdf.wikipathways.org/Pathway/WP5173_r124893/WP/Interaction/e0131 Wikidata Q22281942

InteractionTests.interactionsWithLabels

Interactions found that involve Labels: 13

http://www.wikipathways.org/instance/WP5173_r124893 "Polyglucosan Body Neuropathy" with graphId eba21
http://www.wikipathways.org/instance/WP5173_r124893 "Glycogen Storage Disease XV" with graphId abc2c
http://www.wikipathways.org/instance/WP5173_r124893 "Congenital Disorder Of Glycosylation, 
type It" with graphId de139
http://www.wikipathways.org/instance/WP5173_r124893 "Galactokinase deficiency" with graphId d2625
http://www.wikipathways.org/instance/WP5173_r124893 "Glycogen Storage 
Disease VI" with graphId ae5e6
http://www.wikipathways.org/instance/WP5173_r124893 "Glycogen Storage Disease 0, Liver" with graphId f124e
http://www.wikipathways.org/instance/WP5173_r124893 "Polyglucosan Body Myopathy 2" with graphId b5440
http://www.wikipathways.org/instance/WP5173_r124893 "intestinal glucose-galactose 
malabsorption" with graphId d61c1
http://www.wikipathways.org/instance/WP5173_r124893 "Uridine diphosphate 
galactose-4-epimerase 
deficiency" with graphId c9ff6
http://www.wikipathways.org/instance/WP5173_r124893 "Glycogen Storage Disease 0, Muscle" with graphId fbaa3
http://www.wikipathways.org/instance/WP5173_r124893 "Glycogen Storage 
Disease IV" with graphId aaa50
http://www.wikipathways.org/instance/WP5173_r124893 "Fanconi-Bickel syndrome" with graphId fd3d0
http://www.wikipathways.org/instance/WP5173_r124893 "Galactosaemia" with graphId a8706

InteractionTests.possibleTranslocations

Interactions between identical nodes: 2

http://www.wikipathways.org/instance/WP5173_r124893 http://rdf.wikipathways.org/Pathway/WP5173_r124893/WP/Interaction/a4ae6 "galactose" (https://identifiers.org/chebi/CHEBI:28260) and 
galactose" (https://identifiers.org/chebi/CHEBI:28260)
http://www.wikipathways.org/instance/WP5173_r124893 http://rdf.wikipathways.org/Pathway/WP5173_r124893/WP/Interaction/f075d "galactose" (https://identifiers.org/chebi/CHEBI:28260) and 
galactose" (https://identifiers.org/chebi/CHEBI:28260)

More details at https://wikipathways.github.io/WikiPathwaysCurator/InteractionTests/possibleTranslocations