Wikidata:Database reports/Constraint violations/P3358
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Constraint violations report for positive prognostic predictor for (Discussion, uses, items, changes, related properties): the presence of the genetic variant helps to prognose good outcome for the disease
Data time stamp: (UTC) — Items processed: 70
The report is generated based on the settings on Property:P3358#P2302.
Updates overwrite this page. Some may already be fixed since the last update: check RecentChangesLinked.
When incremental dumps and the bot work as planned, items fixed before 07:00 UTC disappear in the next update. The report is not updated if only the item count changes.
The report can include false positives. There is no need to "fix" them.
Data time stamp: (UTC) — Items processed: 70
The report is generated based on the settings on Property:P3358#P2302.
Updates overwrite this page. Some may already be fixed since the last update: check RecentChangesLinked.
When incremental dumps and the bot work as planned, items fixed before 07:00 UTC disappear in the next update. The report is not updated if only the item count changes.
The report can include false positives. There is no need to "fix" them.
"Scope" violations[edit]
Violations count: 0
"Value type disease (Q12136)" violations[edit]
Violations count: 0
Types statistics[edit]
"Entity types" violations[edit]
Violations count: 0
"Type sequence variant (Q15304597)" violations[edit]
Violations count: 8
- FLT3 TKD MUTATION (Q28381821): Nonsynonymous Variant (Q27905684)
- ABCB1 I1145I (Q28421333): Synonymous Variant (Q28419125)
- MDM2 RS34886328 (Q28423328): 3 Prime UTR Truncation (Q28419139)
- FGFR1 Amplification (Q28444992): Transcript Amplification (Q27907091)
- GNAS c.393T>C (Q29938321): Synonymous Variant (Q28419125)
- PIK3CA EXON 20 MUTATION (Q56241010):
- MYB AMPLIFICATION (Q86217009):
- PIK3CA Rare Mutation (Q102214202):
Types statistics[edit]
Accepted | Type | Usage |
---|---|---|
Yes | sequence variant (Q15304597) | 19 |
Yes | missense mutation (Q2656896) | 12 |
Yes | transcript fusion (Q28419128) | 8 |
Yes | Protein Altering Variant (Q27907087) | 7 |
Yes | Loss Of Function Variant (Q27907094) | 7 |
Yes | transcript variant (Q28371782) | 5 |
Yes | gene variant (Q28381983) | 4 |
Yes | exon variant (Q27908063) | 3 |
Yes | Gain Of Function Variant (Q28371786) | 2 |
No | Synonymous Variant (Q28419125) | 2 |
No | Nonsynonymous Variant (Q27905684) | 1 |
No | Transcript Amplification (Q27907091) | 1 |
Yes | inframe variant (Q28419132) | 1 |
Yes | Polymorphic Sequence Variant (Q28419136) | 1 |
No | 3 Prime UTR Truncation (Q28419139) | 1 |