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KFPT:PT-JP972V1C CUI (KFPT)

Description: A kfpt in the knowledge graph

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CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View KFPT:PT-JP972V1C CUI's neighborhood in the knowledge graph.

Knowledge Graph Assertions

	Source	Relation	Target	Evidence
	KFPT:PT-JP972V1C CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Arnold Chiari Malformation Disease or Phenotype (Entity type)
	KFPT:PT-JP972V1C CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital scar Disease or Phenotype (Entity type)
	KFPT:PT-JP972V1C CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Preauricular dimple Disease or Phenotype (Entity type)
	KFPT:PT-JP972V1C CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Hydrocephalus Disease or Phenotype (Entity type)
	KFPT:PT-JP972V1C CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Left ventricular abnormality Disease or Phenotype (Entity type)
	KFPT:PT-JP972V1C CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Port-Wine Stain Disease or Phenotype (Entity type)
	KFPT:PT-JP972V1C CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Bifid scrotum Disease or Phenotype (Entity type)
	KFPT:PT-JP972V1C CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormal pulmonary vein morphology Disease or Phenotype (Entity type)
	KFPT:PT-JP972V1C CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital blindness Disease or Phenotype (Entity type)
	KFPT:PT-JP972V1C CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Left Isomerism Disease or Phenotype (Entity type)

KFPT:PT-JP972V1C CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Arnold Chiari Malformation
Disease or Phenotype (Entity type)

KFPT:PT-JP972V1C CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital scar
Disease or Phenotype (Entity type)

KFPT:PT-JP972V1C CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Preauricular dimple
Disease or Phenotype (Entity type)

KFPT:PT-JP972V1C CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Hydrocephalus
Disease or Phenotype (Entity type)

KFPT:PT-JP972V1C CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Left ventricular abnormality
Disease or Phenotype (Entity type)

KFPT:PT-JP972V1C CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Port-Wine Stain
Disease or Phenotype (Entity type)

KFPT:PT-JP972V1C CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Bifid scrotum
Disease or Phenotype (Entity type)

KFPT:PT-JP972V1C CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormal pulmonary vein morphology
Disease or Phenotype (Entity type)

KFPT:PT-JP972V1C CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital blindness
Disease or Phenotype (Entity type)

KFPT:PT-JP972V1C CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Left Isomerism
Disease or Phenotype (Entity type)

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The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

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Community

Resources

The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

@CFDE Workbench 2025