| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-125 |
Sentence |
denotes |
Structural characterization of gangliosides isolated from mullet milt using electrospray ionization-tandem mass spectrometry. |
| T1 |
0-125 |
Sentence |
denotes |
Structural characterization of gangliosides isolated from mullet milt using electrospray ionization-tandem mass spectrometry. |
| T1 |
0-125 |
Sentence |
denotes |
Structural characterization of gangliosides isolated from mullet milt using electrospray ionization-tandem mass spectrometry. |
| TextSentencer_T2 |
126-429 |
Sentence |
denotes |
Electrospray ionization (ESI) coupled with tandem mass spectrometry has been used in conjunction with microwave-mediated saponification, periodate oxidation, and clostridial sialidase hydrolysis to enable detailed structural characterization of gangliosides and their derivatives present in mullet milt. |
| T2 |
126-429 |
Sentence |
denotes |
Electrospray ionization (ESI) coupled with tandem mass spectrometry has been used in conjunction with microwave-mediated saponification, periodate oxidation, and clostridial sialidase hydrolysis to enable detailed structural characterization of gangliosides and their derivatives present in mullet milt. |
| T2 |
126-429 |
Sentence |
denotes |
Electrospray ionization (ESI) coupled with tandem mass spectrometry has been used in conjunction with microwave-mediated saponification, periodate oxidation, and clostridial sialidase hydrolysis to enable detailed structural characterization of gangliosides and their derivatives present in mullet milt. |
| TextSentencer_T3 |
430-551 |
Sentence |
denotes |
The gangliosides extracted from mullet milt were determined to be GM3, GM3 lactone, GM3 methyl ester, and 9-O-acetyl GM3. |
| T3 |
430-551 |
Sentence |
denotes |
The gangliosides extracted from mullet milt were determined to be GM3, GM3 lactone, GM3 methyl ester, and 9-O-acetyl GM3. |
| T3 |
430-551 |
Sentence |
denotes |
The gangliosides extracted from mullet milt were determined to be GM3, GM3 lactone, GM3 methyl ester, and 9-O-acetyl GM3. |
| TextSentencer_T4 |
552-663 |
Sentence |
denotes |
For the major ganglioside GM3 and all GM3 derivatives, the ceramide composition was revealed to be C18:1/C16:0. |
| T4 |
552-663 |
Sentence |
denotes |
For the major ganglioside GM3 and all GM3 derivatives, the ceramide composition was revealed to be C18:1/C16:0. |
| T4 |
552-663 |
Sentence |
denotes |
For the major ganglioside GM3 and all GM3 derivatives, the ceramide composition was revealed to be C18:1/C16:0. |
| TextSentencer_T5 |
664-734 |
Sentence |
denotes |
GM3 with a C18:0/C16:0 ceramide was also found as a minor ganglioside. |
| T5 |
664-734 |
Sentence |
denotes |
GM3 with a C18:0/C16:0 ceramide was also found as a minor ganglioside. |
| T5 |
664-734 |
Sentence |
denotes |
GM3 with a C18:0/C16:0 ceramide was also found as a minor ganglioside. |
| TextSentencer_T6 |
735-977 |
Sentence |
denotes |
Both the ganglioside intramolecular ester and the ganglioside methyl ester (lacking carboxylic acid groups) showed dominant chloride attachment peaks (M + Cl)- in negative ion ESI-MS in addition to low intensity peaks corresponding to (M-H)-. |
| T6 |
735-977 |
Sentence |
denotes |
Both the ganglioside intramolecular ester and the ganglioside methyl ester (lacking carboxylic acid groups) showed dominant chloride attachment peaks (M + Cl)- in negative ion ESI-MS in addition to low intensity peaks corresponding to (M-H)-. |
| T6 |
735-977 |
Sentence |
denotes |
Both the ganglioside intramolecular ester and the ganglioside methyl ester (lacking carboxylic acid groups) showed dominant chloride attachment peaks (M + Cl)- in negative ion ESI-MS in addition to low intensity peaks corresponding to (M-H)-. |
| TextSentencer_T7 |
978-1052 |
Sentence |
denotes |
GM3 and O-acetyl GM3 bearing carboxylic acid functions showed only (M-H)-. |
| T7 |
978-1052 |
Sentence |
denotes |
GM3 and O-acetyl GM3 bearing carboxylic acid functions showed only (M-H)-. |
| T7 |
978-1052 |
Sentence |
denotes |
GM3 and O-acetyl GM3 bearing carboxylic acid functions showed only (M-H)-. |
| TextSentencer_T8 |
1053-1344 |
Sentence |
denotes |
In positive ion ESI, GM3 and O-acetyl GM3 revealed (M + 2Na-H)+ peaks in addition to (M + Na)+, indicating free exchange of the carboxylic acid proton with a sodium cation, while the ganglioside intramolecular ester and ganglioside methyl ester with no acidic protons yielded only (M + Na)+. |
| T8 |
1053-1344 |
Sentence |
denotes |
In positive ion ESI, GM3 and O-acetyl GM3 revealed (M + 2Na-H)+ peaks in addition to (M + Na)+, indicating free exchange of the carboxylic acid proton with a sodium cation, while the ganglioside intramolecular ester and ganglioside methyl ester with no acidic protons yielded only (M + Na)+. |
| T8 |
1053-1344 |
Sentence |
denotes |
In positive ion ESI, GM3 and O-acetyl GM3 revealed (M + 2Na-H)+ peaks in addition to (M + Na)+, indicating free exchange of the carboxylic acid proton with a sodium cation, while the ganglioside intramolecular ester and ganglioside methyl ester with no acidic protons yielded only (M + Na)+. |
| TextSentencer_T9 |
1345-1515 |
Sentence |
denotes |
The strategy of employing ESI-MS to detect products of established wet chemical reactions represents a general approach for elucidation of ganglioside structural details. |
| T9 |
1345-1515 |
Sentence |
denotes |
The strategy of employing ESI-MS to detect products of established wet chemical reactions represents a general approach for elucidation of ganglioside structural details. |
| T9 |
1345-1515 |
Sentence |
denotes |
The strategy of employing ESI-MS to detect products of established wet chemical reactions represents a general approach for elucidation of ganglioside structural details. |