FRINK Linked Data Fragments server

Matches in Ubergraph for { <http://purl.obolibrary.org/obo/HP_0005352> ?p ?o ?g. }

• HP_0005352 RO_0002323 PATO_0002062 @default.
• HP_0005352 RO_0002323 PATO_0002301 @default.
• HP_0005352 RO_0002323 PATO_0002302 @default.
• HP_0005352 RO_0002323 TO_0000283 @default.
• HP_0005352 RO_0002323 TO_0000387 @default.
• HP_0005352 UPHENO_0000001 BFO_0000001 @default.
• HP_0005352 UPHENO_0000001 BFO_0000002 @default.
• HP_0005352 UPHENO_0000001 BFO_0000003 @default.
• HP_0005352 UPHENO_0000001 BFO_0000004 @default.
• HP_0005352 UPHENO_0000001 BFO_0000015 @default.
• HP_0005352 UPHENO_0000001 BFO_0000040 @default.
• HP_0005352 UPHENO_0000001 CARO_0000000 @default.
• HP_0005352 UPHENO_0000001 CARO_0000006 @default.
• HP_0005352 UPHENO_0000001 CARO_0020000 @default.
• HP_0005352 UPHENO_0000001 COB_0000006 @default.
• HP_0005352 UPHENO_0000001 COB_0000034 @default.
• HP_0005352 UPHENO_0000001 COB_0000037 @default.
• HP_0005352 UPHENO_0000001 FYPO_0000001 @default.
• HP_0005352 UPHENO_0000001 GO_0002376 @default.
• HP_0005352 UPHENO_0000001 GO_0006955 @default.
• HP_0005352 UPHENO_0000001 GO_0008150 @default.
• HP_0005352 UPHENO_0000001 GO_0050896 @default.
• HP_0005352 UPHENO_0000001 UBERON_0000465 @default.
• HP_0005352 UPHENO_0000001 UBERON_0001062 @default.
• HP_0005352 UPHENO_0000001 UBERON_0002405 @default.
• HP_0005352 UPHENO_0000001 UBERON_0015203 @default.
• HP_0005352 UPHENO_0000001 UBERON_0034923 @default.
• HP_0005352 normalizedInformationContent "100" @default.
• HP_0005352 referenceCount "1" @default.
• HP_0005352 hasDbXref "UMLS:C4025208" @default.
• HP_0005352 hasExactSynonym "Severe T-cell immunodeficiency" @default.
• HP_0005352 id "HP:0005352" @default.
• HP_0005352 type Class @default.
• HP_0005352 comment "Several diseases are classified as severe T cell immunodeficiencies: severe combined immunodeficiency syndrome (SCID), reticular dysgenesis, thymic dysplasia (Nezelof syndrome), combined immunodeficiency disease (CID), and Wiskott-Aldrich syndrome (WAS)." @default.
• HP_0005352 isDefinedBy hp.owl @default.
• HP_0005352 label "Severe T-cell immunodeficiency" @default.
• HP_0005352 subClassOf BFO_0000001 @default.
• HP_0005352 subClassOf BFO_0000002 @default.
• HP_0005352 subClassOf BFO_0000020 @default.
• HP_0005352 subClassOf COB_0000502 @default.
• HP_0005352 subClassOf FBcv_0000000 @default.
• HP_0005352 subClassOf FBcv_0000013 @default.
• HP_0005352 subClassOf FBcv_0000347 @default.
• HP_0005352 subClassOf FBcv_0000448 @default.
• HP_0005352 subClassOf FBcv_0000807 @default.
• HP_0005352 subClassOf FBcv_0001347 @default.
• HP_0005352 subClassOf FYPO_0000001 @default.
• HP_0005352 subClassOf FYPO_0000300 @default.
• HP_0005352 subClassOf FYPO_0001985 @default.
• HP_0005352 subClassOf FYPO_0005447 @default.
• HP_0005352 subClassOf HP_0000001 @default.
• HP_0005352 subClassOf HP_0000118 @default.
• HP_0005352 subClassOf HP_0002715 @default.
• HP_0005352 subClassOf HP_0002721 @default.
• HP_0005352 subClassOf HP_0005352 @default.
• HP_0005352 subClassOf HP_0005374 @default.
• HP_0005352 subClassOf HP_0010978 @default.
• HP_0005352 subClassOf MP_0000001 @default.
• HP_0005352 subClassOf MP_0001790 @default.
• HP_0005352 subClassOf MP_0005387 @default.
• HP_0005352 subClassOf PATO_0000001 @default.
• HP_0005352 subClassOf UPHENO_0001001 @default.
• HP_0005352 subClassOf WBPhenotype_0000519 @default.
• HP_0005352 subClassOf WBPhenotype_0000886 @default.
• HP_0005352 category Attribute @default.
• HP_0005352 category BiologicalEntity @default.
• HP_0005352 category DiseaseOrPhenotypicFeature @default.
• HP_0005352 category Entity @default.
• HP_0005352 category NamedThing @default.
• HP_0005352 category OntologyClass @default.
• HP_0005352 category OrganismAttribute @default.
• HP_0005352 category PathologicalEntityMixin @default.
• HP_0005352 category PhenotypicFeature @default.
• HP_0005352 category PhenotypicQuality @default.
• HP_0005352 category ThingWithTaxon @default.

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