http://dbpedia.org/ontology/abstract
|
Neutrophil immunodeficiency syndrome is a condition caused by mutations in the Rac2 gene.
|
http://dbpedia.org/ontology/icd10
|
D71
|
http://dbpedia.org/ontology/meshId
|
C564275
|
http://dbpedia.org/ontology/omim
|
608203
|
http://dbpedia.org/ontology/orpha
|
183707
|
http://dbpedia.org/ontology/wikiPageID
|
27647850
|
http://dbpedia.org/ontology/wikiPageLength
|
1903
|
http://dbpedia.org/ontology/wikiPageRevisionID
|
994930059
|
http://dbpedia.org/ontology/wikiPageWikiLink
|
http://dbpedia.org/resource/Category:Noninfectious_immunodeficiency-related_cutaneous_conditions +
, http://dbpedia.org/resource/List_of_cutaneous_conditions +
, http://dbpedia.org/resource/Rac2 +
, http://dbpedia.org/resource/Category:Congenital_defects_of_phagocyte_number%2C_function%2C_or_both +
, http://dbpedia.org/resource/Category:Syndromes +
, http://dbpedia.org/resource/Chronic_granulomatous_disease +
, http://dbpedia.org/resource/Immunodeficiency_with_hyper-IgM +
|
http://dbpedia.org/property/field
|
immunology
|
http://dbpedia.org/property/frequency
|
<1 / 1 000 000
|
http://dbpedia.org/property/icd
|
D71
|
http://dbpedia.org/property/meshid
|
564275.0
|
http://dbpedia.org/property/name
|
Neutrophil immunodeficiency syndrome
|
http://dbpedia.org/property/omim
|
608203
|
http://dbpedia.org/property/orphanet
|
183707
|
http://dbpedia.org/property/snomedCt
|
723443003
|
http://dbpedia.org/property/wikiPageUsesTemplate
|
http://dbpedia.org/resource/Template:Reflist +
, http://dbpedia.org/resource/Template:Monocyte_and_granulocyte_disease +
, http://dbpedia.org/resource/Template:Dermatology-stub +
, http://dbpedia.org/resource/Template:Medical_resources +
, http://dbpedia.org/resource/Template:Infobox_medical_condition_%28new%29 +
, http://dbpedia.org/resource/Template:Deficiencies_of_intracellular_signaling_peptides_and_proteins +
|
http://purl.org/dc/terms/subject
|
http://dbpedia.org/resource/Category:Congenital_defects_of_phagocyte_number%2C_function%2C_or_both +
, http://dbpedia.org/resource/Category:Syndromes +
, http://dbpedia.org/resource/Category:Noninfectious_immunodeficiency-related_cutaneous_conditions +
|
http://purl.org/linguistics/gold/hypernym
|
http://dbpedia.org/resource/Condition +
|
http://www.w3.org/ns/prov#wasDerivedFrom
|
http://en.wikipedia.org/wiki/Neutrophil_immunodeficiency_syndrome?oldid=994930059&ns=0 +
|
http://xmlns.com/foaf/0.1/isPrimaryTopicOf
|
http://en.wikipedia.org/wiki/Neutrophil_immunodeficiency_syndrome +
|
http://xmlns.com/foaf/0.1/name
|
Neutrophil immunodeficiency syndrome
|
owl:sameAs |
http://dbpedia.org/resource/Neutrophil_immunodeficiency_syndrome +
, http://www.wikidata.org/entity/Q7003142 +
, http://rdf.freebase.com/ns/m.0c3xb_j +
, http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/834 +
, https://global.dbpedia.org/id/4sRxw +
, http://yago-knowledge.org/resource/Neutrophil_immunodeficiency_syndrome +
|
rdf:type |
http://dbpedia.org/class/yago/Attribute100024264 +
, http://dbpedia.org/class/yago/State100024720 +
, http://dbpedia.org/class/yago/Abstraction100002137 +
, http://dbpedia.org/class/yago/Anomaly114505821 +
, http://dbpedia.org/class/yago/PathologicalState114051917 +
, http://dbpedia.org/class/yago/Abnormality114501726 +
, http://dbpedia.org/class/yago/Illness114061805 +
, http://dbpedia.org/class/yago/Condition113920835 +
, http://dbpedia.org/class/yago/BirthDefect114465048 +
, http://dbpedia.org/class/yago/IllHealth114052046 +
, http://dbpedia.org/ontology/Disease +
, http://dbpedia.org/class/yago/Imperfection114462666 +
, http://dbpedia.org/class/yago/Defect114464005 +
, http://www.wikidata.org/entity/Q12136 +
, http://dbpedia.org/class/yago/PhysicalCondition114034177 +
, http://dbpedia.org/class/yago/Disease114070360 +
, http://dbpedia.org/class/yago/WikicatCongenitalDefectsOfPhagocyteNumber%2CFunction%2COrBoth +
, http://dbpedia.org/class/yago/WikicatNoninfectiousImmunodeficiency-relatedCutaneousConditions +
|
rdfs:comment |
Neutrophil immunodeficiency syndrome is a condition caused by mutations in the Rac2 gene.
|
rdfs:label |
Neutrophil immunodeficiency syndrome
|