Id |
Subject |
Object |
Predicate |
Lexical cue |
T1 |
0-121 |
Sentence |
denotes |
Identification of novel single nucleotide polymorphisms associated with acute respiratory distress syndrome by exome-seq. |
T1 |
0-121 |
Sentence |
denotes |
Identification of novel single nucleotide polymorphisms associated with acute respiratory distress syndrome by exome-seq. |
T2 |
122-333 |
Sentence |
denotes |
Acute respiratory distress syndrome (ARDS) is a lung condition characterized by impaired gas exchange with systemic release of inflammatory mediators, causing pulmonary inflammation, vascular leak and hypoxemia. |
T2 |
122-333 |
Sentence |
denotes |
Acute respiratory distress syndrome (ARDS) is a lung condition characterized by impaired gas exchange with systemic release of inflammatory mediators, causing pulmonary inflammation, vascular leak and hypoxemia. |
T3 |
334-419 |
Sentence |
denotes |
Existing biomarkers have limited effectiveness as diagnostic and therapeutic targets. |
T3 |
334-419 |
Sentence |
denotes |
Existing biomarkers have limited effectiveness as diagnostic and therapeutic targets. |
T4 |
420-562 |
Sentence |
denotes |
To identify disease-associating variants in ARDS patients, whole-exome sequencing was performed on 96 ARDS patients, detecting 1,382,399 SNPs. |
T4 |
420-562 |
Sentence |
denotes |
To identify disease-associating variants in ARDS patients, whole-exome sequencing was performed on 96 ARDS patients, detecting 1,382,399 SNPs. |
T5 |
563-738 |
Sentence |
denotes |
By comparing these exome data to those of the 1000 Genomes Project, we identified a number of single nucleotide polymorphisms (SNP) which are potentially associated with ARDS. |
T5 |
563-738 |
Sentence |
denotes |
By comparing these exome data to those of the 1000 Genomes Project, we identified a number of single nucleotide polymorphisms (SNP) which are potentially associated with ARDS. |
T6 |
739-849 |
Sentence |
denotes |
50,190SNPs were found in all case subgroups and controls, of which89 SNPs were associated with susceptibility. |
T6 |
739-849 |
Sentence |
denotes |
50,190SNPs were found in all case subgroups and controls, of which89 SNPs were associated with susceptibility. |
T7 |
850-1590 |
Sentence |
denotes |
We validated three SNPs (rs78142040, rs9605146 and rs3848719) in additional ARDS patients to substantiate their associations with susceptibility, severity and outcome of ARDS. rs78142040 (C>T) occurs within a histone mark (intron 6) of the Arylsulfatase D gene. rs9605146 (G>A) causes a deleterious coding change (proline to leucine) in the XK, Kell blood group complex subunit-related family, member 3 gene. rs3848719 (G>A) is a synonymous SNP in the Zinc-Finger/Leucine-Zipper Co-Transducer NIF1 gene. rs78142040, rs9605146, and rs3848719 are associated significantly with susceptibility to ARDS. rs3848719 is associated with APACHE II score quartile. rs78142040 is associated with 60-day mortality in the overall ARDS patient population. |
T7 |
850-1590 |
Sentence |
denotes |
We validated three SNPs (rs78142040, rs9605146 and rs3848719) in additional ARDS patients to substantiate their associations with susceptibility, severity and outcome of ARDS. rs78142040 (C>T) occurs within a histone mark (intron 6) of the Arylsulfatase D gene. rs9605146 (G>A) causes a deleterious coding change (proline to leucine) in the XK, Kell blood group complex subunit-related family, member 3 gene. rs3848719 (G>A) is a synonymous SNP in the Zinc-Finger/Leucine-Zipper Co-Transducer NIF1 gene. rs78142040, rs9605146, and rs3848719 are associated significantly with susceptibility to ARDS. rs3848719 is associated with APACHE II score quartile. rs78142040 is associated with 60-day mortality in the overall ARDS patient population. |
T8 |
1591-1666 |
Sentence |
denotes |
Exome-seq is a powerful tool to identify potential new biomarkers for ARDS. |
T8 |
1591-1666 |
Sentence |
denotes |
Exome-seq is a powerful tool to identify potential new biomarkers for ARDS. |
T9 |
1667-1811 |
Sentence |
denotes |
We selectively validated three SNPs which have not been previously associated with ARDS and represent potential new genetic biomarkers for ARDS. |
T9 |
1667-1811 |
Sentence |
denotes |
We selectively validated three SNPs which have not been previously associated with ARDS and represent potential new genetic biomarkers for ARDS. |
T10 |
1812-1937 |
Sentence |
denotes |
Additional validation in larger patient populations and further exploration of underlying molecular mechanisms are warranted. |
T10 |
1812-1937 |
Sentence |
denotes |
Additional validation in larger patient populations and further exploration of underlying molecular mechanisms are warranted. |