| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-5 |
Protein |
denotes |
KCNQ4 |
| T2 |
15-32 |
Protein |
denotes |
potassium channel |
| E1 |
33-42 |
GeneExpression |
denotes |
expressed |
| T4 |
46-70 |
Cell |
denotes |
sensory outer hair cells |
| E2 |
75-82 |
Mutation |
denotes |
mutated |
| E3 |
86-103 |
Disease |
denotes |
dominant deafness |
| T7 |
105-123 |
Protein |
denotes |
Potassium channels |
| E4 |
124-132 |
RegulatoryProcess |
denotes |
regulate |
| E20 |
124-132 |
RegulatoryProcess |
denotes |
regulate |
| T9 |
133-143 |
Ion |
denotes |
electrical |
| E5 |
144-153 |
SignalingPathway |
denotes |
signaling |
| T11 |
162-167 |
Ion |
denotes |
ionic |
| E18 |
168-200 |
CellHomeostasis |
denotes |
composition of biological fluids |
| E6 |
202-211 |
Mutation |
denotes |
Mutations |
| T13 |
231-236 |
Gene |
denotes |
genes |
| T14 |
244-248 |
Protein |
denotes |
KCNQ |
| T15 |
263-278 |
Gene |
denotes |
K+ channel gene |
| E7 |
295-324 |
Disease |
denotes |
inherited cardiac arrhythmias |
| E8 |
356-364 |
Disease |
denotes |
deafness |
| E19 |
370-387 |
Disease |
denotes |
neonatal epilepsy |
| T18 |
408-413 |
Protein |
denotes |
KCNQ4 |
| T38 |
461-472 |
Locus |
denotes |
DFNA2 locus |
| E9 |
487-517 |
Disease |
denotes |
nonsyndromic dominant deafness |
| T20 |
526-533 |
Tissue |
denotes |
cochlea |
| E10 |
541-550 |
GeneExpression |
denotes |
expressed |
| T22 |
554-578 |
Cell |
denotes |
sensory outer hair cells |
| E11 |
582-590 |
Mutation |
denotes |
mutation |
| T24 |
599-603 |
Gene |
denotes |
gene |
| T39 |
609-614 |
Locus |
denotes |
DFNA2 |
| T25 |
649-654 |
Protein |
denotes |
KCNQ4 |
| E12 |
671-680 |
NegativeRegulation |
denotes |
abolishes |
| T40 |
685-694 |
Ion |
denotes |
potassium |
| T27 |
707-722 |
Protein |
denotes |
wild-type KCNQ4 |
| E13 |
785-794 |
Mutation |
denotes |
mutations |
| T29 |
798-803 |
Protein |
denotes |
KCNQ1 |
| E14 |
810-818 |
Disease |
denotes |
deafness |
| E15 |
822-831 |
Affecting |
denotes |
affecting |
| E16 |
832-851 |
CellularProcess |
denotes |
endolymph secretion |
| T33 |
878-883 |
Protein |
denotes |
KCNQ4 |
| E17 |
892-904 |
Disease |
denotes |
hearing loss |
| T35 |
921-937 |
Cell |
denotes |
outer hair cells |
| R1 |
E1 |
T4 |
locatedIn |
expressed,sensory outer hair cells |
| R10 |
E5 |
E4 |
hasPatient |
signaling,regulate |
| R11 |
T13 |
E6 |
hasPatient |
genes,Mutations |
| R12 |
T24 |
E11 |
hasPatient |
gene,mutation |
| R13 |
T29 |
E13 |
hasPatient |
KCNQ1,mutations |
| R14 |
E15 |
E14 |
hasAgent |
affecting,deafness |
| R15 |
E13 |
E15 |
hasAgent |
mutations,affecting |
| R16 |
E16 |
E15 |
hasPatient |
endolymph secretion,affecting |
| R17 |
T33 |
E17 |
hasAgent |
KCNQ4,hearing loss |
| R18 |
E6 |
E7 |
hasAgent |
Mutations,inherited cardiac arrhythmias |
| R19 |
E6 |
E19 |
hasAgent |
Mutations,neonatal epilepsy |
| R2 |
T13 |
T14 |
encodes |
genes,KCNQ |
| R20 |
T7 |
E20 |
hasAgent |
Potassium channels,regulate |
| R21 |
E18 |
E20 |
hasPatient |
composition of biological fluids,regulate |
| R3 |
T22 |
T20 |
locatedIn |
sensory outer hair cells,cochlea |
| R4 |
E10 |
T22 |
locatedIn |
expressed,sensory outer hair cells |
| R5 |
E17 |
T35 |
locatedIn |
hearing loss,outer hair cells |
| R7 |
T1 |
E1 |
hasPatient |
KCNQ4,expressed |
| R8 |
T24 |
T39 |
locatedIn |
gene,DFNA2 |
| R8 |
T1 |
E2 |
hasPatient |
KCNQ4,mutated |
| R9 |
T7 |
E4 |
hasAgent |
Potassium channels,regulate |
