KFPT:PT-02A5YNB1 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-02A5YNB1 CUI's neighborhood in the knowledge graph.

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Knowledge Graph Assertions

Source	Relation	Target
KFPT:PT-02A5YNB1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormality of the hepatic vasculature Disease or Phenotype (Entity type)
KFPT:PT-02A5YNB1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital blindness Disease or Phenotype (Entity type)
KFPT:PT-02A5YNB1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Retinal vascular tortuosity Disease or Phenotype (Entity type)
KFPT:PT-02A5YNB1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormal ventricular septum morphology Disease or Phenotype (Entity type)
KFPT:PT-02A5YNB1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormality of abdominal situs Disease or Phenotype (Entity type)
KFPT:PT-02A5YNB1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Tetralogy of Fallot Disease or Phenotype (Entity type)
KFPT:PT-02A5YNB1 CUI KFPT (Entity type)	Belongs to cohort Knowledge Graph Relation (Entity type)	Kids First: Congenital Heart Defects KFCOHORT (Entity type)
KFPT:PT-02A5YNB1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Hypoplastic Left Heart Syndrome Disease or Phenotype (Entity type)
KFPT:PT-02A5YNB1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Microcephaly (physical finding) Disease or Phenotype (Entity type)
KFPT:PT-02A5YNB1 CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Abnormal ventriculoarterial connection Disease or Phenotype (Entity type)

KFPT:PT-02A5YNB1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormality of the hepatic vasculature
Disease or Phenotype (Entity type)

KFPT:PT-02A5YNB1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital blindness
Disease or Phenotype (Entity type)

KFPT:PT-02A5YNB1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Retinal vascular tortuosity
Disease or Phenotype (Entity type)

KFPT:PT-02A5YNB1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormal ventricular septum morphology
Disease or Phenotype (Entity type)

KFPT:PT-02A5YNB1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormality of abdominal situs
Disease or Phenotype (Entity type)

KFPT:PT-02A5YNB1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Tetralogy of Fallot
Disease or Phenotype (Entity type)

KFPT:PT-02A5YNB1 CUI
KFPT (Entity type)
Belongs to cohort
Knowledge Graph Relation (Entity type)
Kids First: Congenital Heart Defects
KFCOHORT (Entity type)

KFPT:PT-02A5YNB1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Hypoplastic Left Heart Syndrome
Disease or Phenotype (Entity type)

KFPT:PT-02A5YNB1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Microcephaly (physical finding)
Disease or Phenotype (Entity type)

KFPT:PT-02A5YNB1 CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Abnormal ventriculoarterial connection
Disease or Phenotype (Entity type)

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