An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Genetic condition that raises the risk of blood clots

Property Value
dbo:description
  • C und S (de)
  • Genetic condition that raises the risk of blood clots (en)
dbo:diseasesDB
  • 32790
dbo:omim
  • 176930 (xsd:integer)
dbo:symptom
dbo:thumbnail
dbo:wikiPageExternalLink
dbo:wikiPageWikiLink
dbp:chromosome
  • 11 (xsd:integer)
dbp:diseasesdb
  • 32790 (xsd:integer)
dbp:frequency
  • 2.0 (dbd:perCent)
dbp:gene
dbp:name
  • Prothrombin G20210A (en)
dbp:omim
  • 176930 (xsd:integer)
dbp:rsid
  • 1799963 (xsd:integer)
dbp:symptoms
dbp:synonyms
  • Prothrombin thrombophilia, factor II mutation, prothrombin mutation, rs1799963, factor II G20210A (en)
dbp:wikiPageUsesTemplate
dct:subject
rdf:type
rdfs:label
  • Prothrombin G20210A (en)
  • Prothrombinmutation G20210A (de)
  • Thrombophilie par mutation G20210A du gène de la prothrombine (fr)
owl:sameAs
prov:wasDerivedFrom
foaf:depiction
foaf:isPrimaryTopicOf
foaf:name
  • Prothrombin G20210A (en)
is dbo:wikiPageRedirects of
is dbo:wikiPageWikiLink of
is foaf:primaryTopic of
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