PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
12110506-1	2002	Evaluation of renal hemodynamics requires estimation of effective renal plasma flow, which is commonly measured by the renal clearance of p-aminohippuric acid (PAH).	p-Aminohippuric Acid	138-158	phenylalanine hydroxylase	Homo sapiens	160-163	
22027505-7	2012	Para-aminohippuric acid (PAH) significantly reduced the intracellular accumulation of AAI in rOAT1-transfected HEK293 cells.	p-Aminohippuric Acid	0-23	phenylalanine hydroxylase	Homo sapiens	25-28	
16086552-1	2005	The role of phenylalanine 4-monooxygenase (PAH) in the S-oxidation of S-carboxymethyl-L-cysteine (SCMC) in the rat has now been well established in rat cytosolic fractions in vitro.	p-Aminohippuric Acid	43-46	phenylalanine hydroxylase	Homo sapiens	12-41	
12009881-1	2002	Previous studies of ferrous wild-type phenylalanine hydroxylase, [Fe(2+)]PAH(T)[], have shown the active site to be a six-coordinate distorted octahedral site.	p-Aminohippuric Acid	73-76	phenylalanine hydroxylase	Homo sapiens	38-63	
2006152-1	1991	A missense mutation has been identified in the human phenylalanine hydroxylase [PAH; phenylalanine 4-monooxygenase; L-phenylalanine, tetrahydrobiopterin:oxygen oxidoreductase (4-hydroxylating), EC 1.14.16.1] gene in a Chinese patient with classic phenylketonuria (PKU).	p-Aminohippuric Acid	80-83	phenylalanine hydroxylase	Homo sapiens	53-78	
11206195-1	2001	The intestinal transport of an organic anion, p-aminohippuric acid (PAH), was studied in Caco-2 cell monolayers and rat intestinal tissue mounted in Ussing chambers.	p-Aminohippuric Acid	46-66	phenylalanine hydroxylase	Homo sapiens	68-71	
9824245-1	1998	A sensitive and specific high-performance liquid chromatographic assay was developed for the simultaneous determination of p-aminohippuric acid (PAH), acetyl-p-aminohippuric acid (aPAH), and iothalamate in human plasma and urine.	p-Aminohippuric Acid	123-143	phenylalanine hydroxylase	Homo sapiens	145-148	
2006152-1	1991	A missense mutation has been identified in the human phenylalanine hydroxylase [PAH; phenylalanine 4-monooxygenase; L-phenylalanine, tetrahydrobiopterin:oxygen oxidoreductase (4-hydroxylating), EC 1.14.16.1] gene in a Chinese patient with classic phenylketonuria (PKU).	p-Aminohippuric Acid	80-83	phenylalanine hydroxylase	Homo sapiens	85-114	
2675639-8	1989	Organic anion (p-aminohippurate; PAH) uptake is driven by exchange for certain divalent organic anions, e.g., glutarate and alpha-ketoglutarate.	p-Aminohippuric Acid	15-31	phenylalanine hydroxylase	Homo sapiens	33-36	
835603-1	1977	In vitro concentrative transport to tritiated p-aminohippuric acid (3H-PAH) was evaluated in renal biopsy specimens from human subjects by section freeze-dry autoradiography.	p-Aminohippuric Acid	46-66	phenylalanine hydroxylase	Homo sapiens	71-74	
13894152-0	1961	Relationship between renal succinoxidase activity and maximal transport rates of paminohippurate (Tm-PAH) in various representative vertebrates.	p-Aminohippuric Acid	81-96	phenylalanine hydroxylase	Homo sapiens	101-104	
32186110-4	2019	The reabsorption of glucose and the excretion of para-aminohippuric acid (PAH) by HK-2 cells were also examined.	p-Aminohippuric Acid	49-72	phenylalanine hydroxylase	Homo sapiens	74-77