| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
25-30 |
GeneOrGeneProduct |
denotes |
LYRM7 |
| T2 |
31-36 |
GeneOrGeneProduct |
denotes |
MZM1L |
| T3 |
65-79 |
DiseaseOrPhenotypicFeature |
denotes |
encephalopathy |
| T4 |
81-96 |
DiseaseOrPhenotypicFeature |
denotes |
lactic acidosis |
| T5 |
109-147 |
DiseaseOrPhenotypicFeature |
denotes |
reduction of mitochondrial complex III |
| T6 |
201-250 |
DiseaseOrPhenotypicFeature |
denotes |
defective complex III (cIII) of the mitochondrial |
| T7 |
309-313 |
GeneOrGeneProduct |
denotes |
cIII |
| T8 |
381-385 |
GeneOrGeneProduct |
denotes |
cIII |
| T9 |
417-422 |
OrganismTaxon |
denotes |
human |
| T10 |
423-428 |
GeneOrGeneProduct |
denotes |
LYRM7 |
| T11 |
429-434 |
GeneOrGeneProduct |
denotes |
MZM1L |
| T12 |
452-457 |
OrganismTaxon |
denotes |
yeast |
| T13 |
458-462 |
GeneOrGeneProduct |
denotes |
MZM1 |
| T14 |
513-517 |
GeneOrGeneProduct |
denotes |
cIII |
| T15 |
529-536 |
OrganismTaxon |
denotes |
patient |
| T16 |
562-576 |
DiseaseOrPhenotypicFeature |
denotes |
encephalopathy |
| T17 |
578-593 |
DiseaseOrPhenotypicFeature |
denotes |
lactic acidosis |
| T18 |
617-632 |
DiseaseOrPhenotypicFeature |
denotes |
cIII deficiency |
| T19 |
710-717 |
SequenceVariant |
denotes |
c.73G>A |
| T20 |
722-727 |
GeneOrGeneProduct |
denotes |
LYRM7 |
| T21 |
728-733 |
GeneOrGeneProduct |
denotes |
MZM1L |
| T22 |
805-815 |
SequenceVariant |
denotes |
p.Asp25Asn |
| T23 |
823-828 |
GeneOrGeneProduct |
denotes |
mzm1Δ |
| T24 |
829-834 |
OrganismTaxon |
denotes |
yeast |
| T25 |
863-867 |
GeneOrGeneProduct |
denotes |
mzm1 |
| T26 |
868-872 |
SequenceVariant |
denotes |
D25N |
| T27 |
917-942 |
DiseaseOrPhenotypicFeature |
denotes |
respiratory growth defect |
| T28 |
954-960 |
ChemicalEntity |
denotes |
oxygen |
| T29 |
1015-1034 |
GeneOrGeneProduct |
denotes |
Rieske Fe-S protein |
| T30 |
1048-1059 |
GeneOrGeneProduct |
denotes |
complex III |
| T31 |
1081-1086 |
GeneOrGeneProduct |
denotes |
LYRM7 |
| T32 |
1087-1092 |
GeneOrGeneProduct |
denotes |
MZM1L |
| T33 |
1126-1140 |
DiseaseOrPhenotypicFeature |
denotes |
cIII-defective |
| T34 |
1162-1190 |
DiseaseOrPhenotypicFeature |
denotes |
mitochondrial encephalopathy |
