Property talk:P1929

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ClinVar Variation ID
identifier in the ClinVar database for human genomic variation

Applicable "stated in" value	ClinVar (Q20023123)
Data type	External identifier
Domain	instance of genetic variation (Q349856) (note: this should be moved to the property statements)
Allowed values	According to this template: RCV000000000.0 - RCV999999999.* (* is an integer representing the release number, will slowly increase with time) According to statements in the property: \d+ When possible, data should only be stored as statements
Example	NM 000492.3(CFTR):c.1521 1523delCTT (p.Phe508delPhe) (Q19888172) → 7105 BRAF V600E (Q21851559) → 13961 NM_000277.2(PAH):c.1A>G (p.Met1Val) (Q64401263) → 586
Source	https://www.ncbi.nlm.nih.gov/clinvar/
Formatter URL	https://www.ncbi.nlm.nih.gov/clinvar/variation/$1/
Robot and gadget jobs	Robots will add and edit the Clinvar Accession Numbers on appropriate WD items
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 Items with no other external identifier 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/P1929 Map Random list
Proposal discussion	Proposal discussion
Current uses	Total 6 Main statement 3 50% of uses Qualifier 3 50% of uses
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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/P1929#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/P1929#Single value, SPARQL

Format “\d+”: 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/P1929#Format, SPARQL

Scope is as main value (Q54828448), as reference (Q54828450): the property must be used by specified way only (Help)

List of violations of this constraint: Database reports/Constraint violations/P1929#Scope, 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/P1929#Entity types

Changed to Clinvar variation ID

Since this property had only one use, and that use incorrectly used the Clinvar accession in place of the variation ID, I've repurposed this property to Clinvar variation ID (e.g. https://www.ncbi.nlm.nih.gov/clinvar/variation/7105/) which points to a specific variant, instead of the accession (e.g. https://www.ncbi.nlm.nih.gov/clinvar/RCV000007523.8/, which points to a variant:phenotype interaction. The one use used an accession # on an item about the variant only. Since we only currently have items about variant and not variant:phenotype interactions, it makes more sense to use the variation ID. The accession could be used down the line. Gstupp (talk) 00:50, 11 November 2017 (UTC)