wikipathways-collection

WikiPathways WP5189

Summary

Fails

Data nodes without an identifier

The following DataNodes have no identifier: 2

http://classic.wikipathways.org/instance/WP5189_r128212 http://rdf.wikipathways.org/Pathway/WP5189_r128212/DataNode/cb8d9 (Reductase)
http://classic.wikipathways.org/instance/WP5189_r128212 http://rdf.wikipathways.org/Pathway/WP5189_r128212/DataNode/fbedb (Reductase)

More details at https://www.wikipathways.org/WikiPathwaysCurator/DataNodesTests/dataNodesWithoutIdentifier

DataNodesTests.unknownTypes

The following DataNodes have Unknown @Type: 2

http://classic.wikipathways.org/instance/WP5189_r128212 http://rdf.wikipathways.org/Pathway/WP5189_r128212/DataNode/cb8d9 (Reductase)
http://classic.wikipathways.org/instance/WP5189_r128212 http://rdf.wikipathways.org/Pathway/WP5189_r128212/DataNode/fbedb (Reductase)

InteractionTests.interactionsWithLabels

Interactions found that involve Labels: 5

http://classic.wikipathways.org/instance/WP5189_r128212 "X-linked distal spinal 
muscular atrophy" with graphId a0156
http://classic.wikipathways.org/instance/WP5189_r128212 "MEDNIK syndrome" with graphId f1b13
http://classic.wikipathways.org/instance/WP5189_r128212 "Occipital horn syndrome" with graphId f0f37
http://classic.wikipathways.org/instance/WP5189_r128212 "Wilson disease" with graphId c84f9
http://classic.wikipathways.org/instance/WP5189_r128212 "Menkes disease" with graphId dfcfd

At least one reference

Found 1 pathways with zero (PubMed) references

* [http://classic.wikipathways.org/instance/WP5189_r128212](http://classic.wikipathways.org/instance/WP5189_r128212) 'Copper metabolism' in Homo sapiens has zero references; 

More details at https://www.wikipathways.org/WikiPathwaysCurator/ReferencesTests/atLeastOneReference