Property talk:P1199

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mode of inheritance
manner in which a particular genetic trait or disorder is passed from one generation to the next

Description	the manner in which a particular genetic trait or disorder is passed from one generation to the next
Represents	mode of inheritance (Q1348351)
Data type	Item
Domain	According to this template: phenotypic trait (Q1211967) According to statements in the property: phenotypic trait (Q1211967) or disease (Q12136) When possible, data should only be stored as statements
Allowed values	mode of inheritance (Q1348351) (latest list), such as autosomal dominant (Q15729063), X-linked recessive (Q1988987), mtDNA transmission (Q15729075)... (note: this should be moved to the property statements)
Example	Bloom syndrome (Q1469646) → autosomal recessive (Q15729064)
Source	Biomedical literature and databases (note: this information should be moved to a property statement; use property source website for the property (P1896))
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) Database reports/Constraint violations/P1199 Map Random list
Proposal discussion	Proposal discussion
Current uses	Total 87 Main statement 85 97.7% of uses Qualifier 2 2.3% of uses
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Single value: this property generally contains a single value. (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/P1199#Single value, SPARQL

Type “phenotypic trait (Q1211967), disease (Q12136)”: item must contain property “instance of (P31), subclass of (P279)” with classes “phenotypic trait (Q1211967), disease (Q12136)” 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/P1199#Type Q1211967, Q12136, SPARQL

Value type “mode of inheritance (Q1348351)”: This property should use items as value that contain property “instance of (P31)”. On these, the value for instance of (P31) should be an item that uses subclass of (P279) with value mode of inheritance (Q1348351) (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/P1199#Value type Q1348351, SPARQL

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/P1199#Scope, hourly updated report, SPARQL