Property talk:P2249

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[create Create a translatable help page (preferably in English) for this property to be included here]
Distinct values: this property likely contains a value that is different from all other items. (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/P2249#Unique value, SPARQL (every item), SPARQL (by value)
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/P2249#Single value, SPARQL
Format “[A-Z]{2}_\d (\.\d{1,2})?: value must be formatted using this pattern (PCRE syntax). (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/P2249#Format, SPARQL
Format “[A-Z]{2}. : value must be formatted using this pattern (PCRE syntax). (Help)
List of violations of this constraint: Database reports/Constraint violations/P2249#Format, hourly updated report, 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/P2249#Entity types

Store version in the ID?

[edit]

Hello. The mouse chromosome 6 (Q15305576) has RefSeq genome ID (P2249) of NC_000072, but also "NC_000072.1", "NC_000072.2", ... up to "NC_000072.6" (as of today). The "version number" increases when the data updates. However, it is still the same genome that is being identified. Therefore I propose to only store the identifier before the point (".") and eventually tighten the regex. Toni 001 (talk) 12:30, 27 March 2020 (UTC)[reply]

Changes in version number can encompass deletions (e.g. miscalled genes) and even sequence insertions (which disrupt position indexing). Dropping the version number can lead to obsolete references in other properties, like "genomic start". Ivanerill (talk) 23:18, 23 December 2022 (UTC)[reply]

Update regex to accommodate newer RefSeq identifiers

[edit]

RefSeq uses identifiers like NZ_CP023401.1, based on the INSDC identifier (CP023401.1) that do not comply with current regex rule. Ivanerill (talk) 23:23, 23 December 2022 (UTC)[reply]