PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
27098211-4	2016	The obtained copolymers (P1 and P2) having desirable water solubility were well-characterized by infrared spectroscopy (IR), nuclear magnetic resonance (NMR), gel permeation chromatography (GPC), UV-Vis absorption spectroscopy, and photoluminescence spectroscopy.	Water	53-58	crystallin gamma F, pseudogene	Homo sapiens	25-34	
2536699-3	1989	Treatment of the (Sp,Sp)-stereoisomer with cyanogen bromide in [18O]water leads to substitution of sulfur by 18O with predominant retention of configuration at P1 and P4. (Sp,Sp)-P1,P4-Bis(5"-adenosyl)-1[thio-18O2],4[thio-18O2]tetraphosphate was synthesized and on treatment with cyanogen bromide in [17O]water gave (Rp,Rp)-P1,P4-bis(5"-adenosyl)-1[17O,18O2],4[17O,18O2]tetraphosphate.	Water	68-73	crystallin gamma F, pseudogene	Homo sapiens	160-170	
2536699-3	1989	Treatment of the (Sp,Sp)-stereoisomer with cyanogen bromide in [18O]water leads to substitution of sulfur by 18O with predominant retention of configuration at P1 and P4. (Sp,Sp)-P1,P4-Bis(5"-adenosyl)-1[thio-18O2],4[thio-18O2]tetraphosphate was synthesized and on treatment with cyanogen bromide in [17O]water gave (Rp,Rp)-P1,P4-bis(5"-adenosyl)-1[17O,18O2],4[17O,18O2]tetraphosphate.	Water	305-310	crystallin gamma F, pseudogene	Homo sapiens	160-170	
3079530-3	1988	The triclinic form (P1, Z = 1) from DMSO/H2O crystallizes as a dihydrate (Karle, Sukumar & Balaram (1986) Proc, Natl, Acad.	Water	41-44	crystallin gamma F, pseudogene	Homo sapiens	20-29	
28842602-2	2017	Here, the self-assembly mechanism of a peptide-perylenediimide (P-1) conjugate in mixed solvent systems of THF/water is studied and the semiconducting properties are correlated with the morphology.	Water	111-116	crystallin gamma F, pseudogene	Homo sapiens	64-67	
24650226-4	2014	It was observed that P1 and P2 displayed different temperature dependent solution properties in water, with P1 forming micelles above the LCST of the PNIPA while P2 showing macroscopic phase separation under similar conditions.	Water	96-101	crystallin gamma F, pseudogene	Homo sapiens	21-30	
1529338-2	1992	Direct experimental support for this hypothesis has been obtained in studies of the condensation of the 5"-phosphorimidazolide of adenosine (ImpA) with itself and with P1,P2-diadenosine-5",5"-pyrophosphate (AppA) in water in the presence of a montmorillonite clay.	Water	216-221	crystallin gamma F, pseudogene	Homo sapiens	168-173	
20386792-1	2010	H-Phosphinic acid and pyruvic acid, both plausible prebiotic chemicals, react selectively in water to build structural complexity including amide bond formation under remarkably mild conditions and oxidative coupling of P(1) compounds to condensed pyrophosphorus compounds.	Water	93-98	crystallin gamma F, pseudogene	Homo sapiens	220-224	
15679399-6	2005	AU-I, [C4N2H14][Zn(HPO4)2].H2O, crystallizes in the triclinic space group P-1, a = 8.215(2), b = 8.810(3), c = 8.861(3) A, alpha = 88.001(4) degrees , beta = 89.818(5) degrees , and gamma = 89.773(5) degrees , Z = 2.	Water	27-30	crystallin gamma F, pseudogene	Homo sapiens	74-77	
1432622-4	1992	The values obtained could be correlated with the values for n-octanol-water partition taken from the literature by an approach based on the linear solvation relationship: log P1 = a log P2 + b; in this relationship, a and b are constants and P1 and P2 correspond to the two different organic and aqueous phase partition equilibria.	Water	70-75	crystallin gamma F, pseudogene	Homo sapiens	242-251	
20060312-3	2010	The more lipophilic nature of triphenylphosphonium ion over triethylammonium ion renders P1 and P2 higher octanol/water partition coefficients than P3 and P4.	Water	114-119	crystallin gamma F, pseudogene	Homo sapiens	89-98