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PubMed:10223112 / 244-540 JSONTXT

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Inflammaging

Id Subject Object Predicate Lexical cue
T3 0-296 Sentence denotes Progressive familial intrahepatic cholestasis (PFIC), also known as Byler disease, is an inherited cholestasis of hepatocellular origin which is characterized by cholestasis presenting often in the neonatal period leading to death due to liver failure at ages ranging from infancy to adolescence.
T3 0-296 Sentence denotes Progressive familial intrahepatic cholestasis (PFIC), also known as Byler disease, is an inherited cholestasis of hepatocellular origin which is characterized by cholestasis presenting often in the neonatal period leading to death due to liver failure at ages ranging from infancy to adolescence.

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 21-45 HP_0001406 denotes intrahepatic cholestasis
T2 34-45 HP_0001396 denotes cholestasis
T3 99-110 HP_0001396 denotes cholestasis
T4 162-173 HP_0001396 denotes cholestasis
T5 238-251 HP_0001399 denotes liver failure