209D58B62912072772219AFC44DE56B9A2D6062E2F53E11D0DC9FB33F32FF3DCDD4A253BF6DEAC7ED04A744D92F938D9

Defects in APOA5 are a cause of susceptibility to familial hypertriglyceridemia (FHTR)[MIM:145750].mFamilial hypertriglyceridemia is a common inherited disorder in which the concentration of very low density lipoprotein (VLDL) is elevated in the plasma. This leads to increased risk of heart disease, obesity, and pancreatitis.

Source:http://purl.uniprot.org/SHA-384/209D58B62912072772219AFC44DE56B9A2D6062E2F53E11D0DC9FB33F32FF3DCDD4A253BF6DEAC7ED04A744D92F938D9

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rdf:type	uniprot:Disease_Annotation
rdfs:comment	Defects in APOA5 are a cause of susceptibility to familial hypertriglyceridemia (FHTR)[MIM:145750].mFamilial hypertriglyceridemia is a common inherited disorder in which the concentration of very low density lipoprotein (VLDL) is elevated in the plasma. This leads to increased risk of heart disease, obesity, and pancreatitis.