KFPT:PT-S3M51MYV 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-S3M51MYV CUI's neighborhood in the knowledge graph.

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Knowledge Graph Assertions

Source	Relation	Target
KFPT:PT-S3M51MYV CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Phenotypic abnormality Disease or Phenotype (Entity type)
KFPT:PT-S3M51MYV CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Facial Paresis Disease or Phenotype (Entity type)
KFPT:PT-S3M51MYV CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Hearing abnormality Disease or Phenotype (Entity type)
KFPT:PT-S3M51MYV CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital anomaly of face Disease or Phenotype (Entity type)
KFPT:PT-S3M51MYV CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Urogenital Diseases Disease or Phenotype (Entity type)
KFPT:PT-S3M51MYV CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Cardiovascular Abnormalities Disease or Phenotype (Entity type)
KFPT:PT-S3M51MYV CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Lower cranial nerve dysfunction Disease or Phenotype (Entity type)
KFPT:PT-S3M51MYV CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Congenital digestive system anomalies Disease or Phenotype (Entity type)
KFPT:PT-S3M51MYV CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Scoliosis, unspecified Disease or Phenotype (Entity type)
KFPT:PT-S3M51MYV CUI KFPT (Entity type)	Has phenotype Knowledge Graph Relation (Entity type)	Imaging of brain abnormal Disease or Phenotype (Entity type)

KFPT:PT-S3M51MYV CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Phenotypic abnormality
Disease or Phenotype (Entity type)

KFPT:PT-S3M51MYV CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Facial Paresis
Disease or Phenotype (Entity type)

KFPT:PT-S3M51MYV CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Hearing abnormality
Disease or Phenotype (Entity type)

KFPT:PT-S3M51MYV CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital anomaly of face
Disease or Phenotype (Entity type)

KFPT:PT-S3M51MYV CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Urogenital Diseases
Disease or Phenotype (Entity type)

KFPT:PT-S3M51MYV CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Cardiovascular Abnormalities
Disease or Phenotype (Entity type)

KFPT:PT-S3M51MYV CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Lower cranial nerve dysfunction
Disease or Phenotype (Entity type)

KFPT:PT-S3M51MYV CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Congenital digestive system anomalies
Disease or Phenotype (Entity type)

KFPT:PT-S3M51MYV CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Scoliosis, unspecified
Disease or Phenotype (Entity type)

KFPT:PT-S3M51MYV CUI
KFPT (Entity type)
Has phenotype
Knowledge Graph Relation (Entity type)
Imaging of brain abnormal
Disease or Phenotype (Entity type)

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