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About:
Prothrombin G20210A
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
dbr
:Thrombus
dbo:
thumbnail
wiki-commons
:Special:FilePath/Classical_blood_coagulation_pathway.png?width=300
dbo:
wikiPageExternalLink
http://th.schattauer.de/en/contents/archive/issue/2275/manuscript/24423/download.html
https://web.archive.org/web/20160610164443/https:/th.schattauer.de/en/contents/archive/issue/2275/manuscript/24423/download.html
dbo:
wikiPageWikiLink
dbr
:Protein_C
dbr
:Thrombin
dbr
:Protein_S
dbr
:Caucasian_race
dbr
:DNA
dbr
:Single-nucleotide_polymorphism
dbr
:Adenine
dbr
:Pulmonary_embolism
dbr
:Guanine
dbr
:Genetic_testing
dbr
:Deep_vein_thrombosis
dbr
:Meta-analysis
dbr
:Blood_type
dbr
:Coagulation
dbr
:Factor_V_Leiden
dbr
:Hyperprothrombinemia
dbr
:Start_codon
dbr
:Post-thrombotic_syndrome
dbr
:Thrombophilia
dbr
:Venous_ulcer
dbr
:Sense_strand
dbc
:Coagulopathies
dbr
:Coronary_disease
dbr
:Hypercoagulability
dbr
:Anticoagulation
dbr
:Blood_clots
dbr
:Genetic_condition
dbr
:F2_gene
dbr
:Noncoding_DNA
dbr
:Prothrombin
dbr
:Arterial_thrombosis
dbr
:Combined_birth_control_pills
dbr
:Factor_II
dbr
:3'_untranslated_region
dbr
:Blood_coagulation
dbr
:Heterozygous
dbr
:Poly-A_tail
dbr
:File:Classical_blood_coagulation_pathway.png
dbp:
chromosome
11
(xsd:integer)
dbp:
diseasesdb
32790
(xsd:integer)
dbp:
frequency
2.0
(dbd:perCent)
dbp:
gene
dbr
:Thrombin
dbp:
name
Prothrombin G20210A
(en)
dbp:
omim
176930
(xsd:integer)
dbp:
rsid
1799963
(xsd:integer)
dbp:
symptoms
dbr
:Thrombus
dbp:
synonyms
Prothrombin thrombophilia, factor II mutation, prothrombin mutation, rs1799963, factor II G20210A
(en)
dbp:
wikiPageUsesTemplate
dbt
:Infobox_single_nucleotide_polymorphism
dbt
:Citation_needed
dbt
:Cite_journal
dbt
:Efn
dbt
:Genetics
dbt
:Infobox_medical_condition_(new)
dbt
:Medical_resources
dbt
:Medicine
dbt
:Notelist
dbt
:Reflist
dct:
subject
dbc
:Coagulopathies
rdf:
type
owl
:Thing
wikidata
:Q12136
dbo
:Disease
dbo
:Disease
dbo
:Disease
rdfs:
label
Prothrombin G20210A
(en)
Prothrombinmutation G20210A
(de)
Thrombophilie par mutation G20210A du gène de la prothrombine
(fr)
owl:
sameAs
freebase
:Prothrombin G20210A
wikidata
:Prothrombin G20210A
dbpedia-de
:Prothrombin G20210A
dbpedia-fr
:Prothrombin G20210A
dbpedia-global
:Prothrombin G20210A
prov:
wasDerivedFrom
wikipedia-en
:Prothrombin_G20210A?oldid=1300122113&ns=0
foaf:
depiction
wiki-commons
:Special:FilePath/Classical_blood_coagulation_pathway.png
foaf:
isPrimaryTopicOf
wikipedia-en
:Prothrombin_G20210A
foaf:
name
Prothrombin G20210A
(en)
is
dbo:
wikiPageRedirects
of
dbr
:Prothrombin_20210A
dbr
:Prothrombin_20210A_variant
dbr
:Prothrombin_20210_mutation
dbr
:Prothrombin_20210a
dbr
:Prothrombin_20210a_mutation
dbr
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dbr
:Prothrombin_gene_mutation
dbr
:Prothrombin_mutation
dbr
:Prothrombin_mutation_G20210A
dbr
:20210A
dbr
:G20210A
dbr
:F2G20210A
dbr
:F2_20210A
dbr
:F2_G20210A
dbr
:Factor_2_mutation
dbr
:Factor_II_G20210A
dbr
:Factor_II_mutation
dbr
:Rs1799963
is
dbo:
wikiPageWikiLink
of
dbr
:Thrombosis
dbr
:Thrombin
dbr
:Recurrent_miscarriage
dbr
:Deep_vein_thrombosis
dbr
:Coagulation
dbr
:Factor_V_Leiden
dbr
:Thrombosis_prevention
dbr
:Genetic_studies_on_Sinhalese
dbr
:Venous_thrombosis
dbr
:May–Thurner_syndrome
dbr
:Hyperprothrombinemia
dbr
:Antiphospholipid_syndrome
dbr
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dbr
:Pre-existing_disease_in_pregnancy
dbr
:Prothrombin_20210A
dbr
:Prothrombin_20210A_variant
dbr
:Prothrombin_20210_mutation
dbr
:Prothrombin_20210a
dbr
:Prothrombin_20210a_mutation
dbr
:Prothrombin_F2G20210A_mutation
dbr
:Prothrombin_gene_mutation
dbr
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dbr
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dbr
:20210A
dbr
:G20210A
dbr
:F2G20210A
dbr
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dbr
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dbr
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dbr
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dbr
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is
foaf:
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