gene variant according to myvariant.info (E103)
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| language code | label | description | aliases | edit |
|---|---|---|---|---|
| en | gene variant according to myvariant.info | schema of gene variant statements sourced through myvariant.info | edit | |
| pl | wariant genu według myvariant.info | edit |
PREFIX wd: <http://www.wikidata.org/entity/>
PREFIX prov: <http://www.w3.org/ns/prov#>
PREFIX pr: <http://www.wikidata.org/prop/reference/>
PREFIX ps: <http://www.wikidata.org/prop/statement/>
PREFIX pq: <http://www.wikidata.org/prop/qualifier/>
PREFIX p: <http://www.wikidata.org/prop/>
PREFIX xsd: <http://www.w3.org/2001/XMLSchema#>
# This schema describes the variant items on Wikidata that are being enriched
# through myvariant.info.
# It currently sources dbSNP and citation mentioned in dbSNP records, but can
# gradually be extended with other properties form myvariant.info
# query_map: SELECT * WHERE {?variant wdt:P3329 ?civicid}
<variant> {
#dbSNP variant id
p:P6861 {
ps:P6861 xsd:string ;
pq:P383 xsd:string ;
};
#described by source
p:P1343 {
ps:P1343 @<pubmed_reference> ;
prov:wasDerivedFrom @<dbSNP_reference> ;
}* # Contains zero or more reference describing this variant.
}
# references
<dbSNP_reference> {
pr:P248 [wd:Q5243761] ;
pr:P813 xsd:dateTime ;
pr:P6861 xsd:string ;
}
<pubmed_reference> {
}