Property talk:P3356

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positive diagnostic predictor for
the presence of the genetic variant helps to diagnose the presence of disease, used as inclusion criteria

Represents	medical diagnosis (Q177719)
Data type	Item
Domain	According to this template: sequence variant (Q15304597) According to statements in the property: sequence variant (Q15304597) When possible, data should only be stored as statements
Example	ABL1 BCR::ABL (Q27653851) → chronic myeloid leukemia (Q729735)
Source	CIViC, ClinVar (note: this information should be moved to a property statement; use property source website for the property (P1896))
Robot and gadget jobs	ProteinBoxBot will update wikidata from authoritative resources on sequence variants.
See also	positive therapeutic predictor for (P3354), negative therapeutic predictor for (P3355), negative diagnostic predictor for (P3357), positive prognostic predictor for (P3358), negative prognostic predictor for (P3359), CIViC variant ID (P3329), HGVS nomenclature (P3331)
Lists	Items with the most statements of this property Count of items by number of statements (chart) Items with the most statements Items with the fewest statements Count of items by number of sitelinks (chart) Items with the most sitelinks Items with the most sitelinks, but no link to one Wikipedia (sample: Welsh Wikipedia, cywiki) Items with the fewest sitelinks Most linked wikis Items with the most identifier properties By value of property Most statements Fewest statements Most sitelinks Most linked wikis Total of sitelinks on items Most identifiers Fewest identifiers Items with no other statements Most recently created items Items with novalue claims Items with unknown value claims Usage history (total) Usage history (main statement) Chart by item creation date Database reports/Constraint violations/P3356 Map Random list
Proposal discussion	Proposal discussion
Current uses	Total 172 Main statement 171 99.4% of uses Qualifier 1 0.6% of uses
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[create Create a translatable help page (preferably in English) for this property to be included here]

Scope is as main value (Q54828448): the property must be used by specified way only (Help)

List of violations of this constraint: Database reports/Constraint violations/P3356#Scope, hourly updated report, SPARQL

Value type “disease (Q12136)”: This property should use items as value that contain property “instance of (P31), subclass of (P279)”. On these, the value for instance of (P31), subclass of (P279) should be an item that uses subclass of (P279) with value disease (Q12136) (or a subclass thereof). (Help)

Exceptions are possible as rare values may exist. Exceptions can be specified using exception to constraint (P2303).
List of violations of this constraint: Database reports/Constraint violations/P3356#Value type Q12136, SPARQL

Type “sequence variant (Q15304597)”: item must contain property “instance of (P31), subclass of (P279)” with classes “sequence variant (Q15304597)” or their subclasses (defined using subclass of (P279)). (Help)

Exceptions are possible as rare values may exist. Exceptions can be specified using exception to constraint (P2303).
List of violations of this constraint: Database reports/Constraint violations/P3356#Type Q15304597, SPARQL

Allowed entity types are Wikibase item (Q29934200): the property may only be used on a certain entity type (Help)

Exceptions are possible as rare values may exist. Exceptions can be specified using exception to constraint (P2303).
List of violations of this constraint: Database reports/Constraint violations/P3356#Entity types

Discussion

Alignment with Relations Ontology

http://purl.obolibrary.org/obo/RO_0002607 or http://purl.obolibrary.org/obo/RO_0003308 ?