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PubMed:10025409 JSONTXT

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bionlp-st-gro-2013-development

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

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 305-324 HP_0011675 denotes cardiac arrhythmias
T2 313-324 HP_0011675 denotes arrhythmias
T3 356-364 HP_0000365 denotes deafness
T4 509-517 HP_0000365 denotes deafness
T5 810-818 HP_0000365 denotes deafness
T6 892-904 HP_0000365 denotes hearing loss

DisGeNET

Id Subject Object Predicate Lexical cue
T0 878-883 gene:9132 denotes KCNQ4
T1 892-904 disease:C0155552 denotes hearing loss
R1 T0 T1 associated_with KCNQ4,hearing loss

Anatomy-MAT

Id Subject Object Predicate Lexical cue mat_id
T1 60-64 Body_part denotes hair http://purl.obolibrary.org/obo/MAT_0000160
T2 526-533 Body_part denotes cochlea http://purl.obolibrary.org/obo/MAT_0000144
T3 568-572 Body_part denotes hair http://purl.obolibrary.org/obo/MAT_0000160
T4 927-931 Body_part denotes hair http://purl.obolibrary.org/obo/MAT_0000160

GlyCosmos15-HP

Id Subject Object Predicate Lexical cue hp_id
T1 95-103 Phenotype denotes deafness HP:0000365
T2 305-324 Phenotype denotes cardiac arrhythmias HP:0011675
T3 356-364 Phenotype denotes deafness HP:0000365
T4 379-387 Phenotype denotes epilepsy HP:0001250
T5 509-517 Phenotype denotes deafness HP:0000365
T6 810-818 Phenotype denotes deafness HP:0000365
T7 892-904 Phenotype denotes hearing loss HP:0000365

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 95-103 Disease denotes deafness http://purl.obolibrary.org/obo/MONDO_0005365
T2 313-324 Disease denotes arrhythmias http://purl.obolibrary.org/obo/MONDO_0007263
T3 356-364 Disease denotes deafness http://purl.obolibrary.org/obo/MONDO_0005365
T4 379-387 Disease denotes epilepsy http://purl.obolibrary.org/obo/MONDO_0005027
T5 509-517 Disease denotes deafness http://purl.obolibrary.org/obo/MONDO_0005365
T6 810-818 Disease denotes deafness http://purl.obolibrary.org/obo/MONDO_0005365
T7 892-904 Disease denotes hearing loss http://purl.obolibrary.org/obo/MONDO_0005365

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T1 60-70 Body_part denotes hair cells http://purl.obolibrary.org/obo/CL_0000855
T2 526-533 Body_part denotes cochlea http://purl.obolibrary.org/obo/UBERON_0001844
T3 568-578 Body_part denotes hair cells http://purl.obolibrary.org/obo/CL_0000855
T4 655-659 Body_part denotes pore http://purl.obolibrary.org/obo/UBERON_0008915
T5 832-841 Body_part denotes endolymph http://purl.obolibrary.org/obo/UBERON_0001852
T6 927-937 Body_part denotes hair cells http://purl.obolibrary.org/obo/CL_0000855

Glycosmos15-CL

Id Subject Object Predicate Lexical cue cl_id
T1 60-70 Cell denotes hair cells http://purl.obolibrary.org/obo/CL:0000374|http://purl.obolibrary.org/obo/CL:0000855
T3 568-578 Cell denotes hair cells http://purl.obolibrary.org/obo/CL:0000374|http://purl.obolibrary.org/obo/CL:0000855
T5 927-937 Cell denotes hair cells http://purl.obolibrary.org/obo/CL:0000374|http://purl.obolibrary.org/obo/CL:0000855