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PubMed:22539006 / 281-502 JSONTXT

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PubTator4TogoVar

Id Subject Object Predicate Lexical cue proteinmutation
22539006_2 30-36 ProteinMutation denotes G2019S rs34637584

c_corpus

Id Subject Object Predicate Lexical cue
T38 38-43 PR:Q5S006 denotes LRRK2
T39 38-43 PR:000003033 denotes LRRK2
T40 38-43 PR:Q5S007 denotes LRRK2
T41 44-54 SO:0000781 denotes transgenic
T42 44-59 10090 denotes transgenic mice
T43 44-59 D008822 denotes transgenic mice
T44 55-59 PR:000005054 denotes mice
T46 55-59 O89094 denotes mice
T49 113-143 UBERON:0001966 denotes substantia nigra pars compacta
T50 113-143 UBERON:0001965 denotes substantia nigra pars compacta
T51 130-134 PR:P07814 denotes pars
T52 130-134 PR:000007144 denotes pars
T54 145-149 PR:Q9U9R7 denotes SNpc
T55 145-149 UBERON:0001965 denotes SNpc
T56 176-188 D020734 denotes parkinsonism
T57 176-188 D020734 denotes parkinsonism

DisGeNET

Id Subject Object Predicate Lexical cue
T0 38-43 gene:120892 denotes LRRK2
T1 176-188 disease:C0242422 denotes parkinsonism
R1 T0 T1 associated_with LRRK2,parkinsonism

PubmedHPO

Id Subject Object Predicate Lexical cue
T2 176-188 HP_0001300 denotes parkinsonism

Allie

Id Subject Object Predicate Lexical cue
SS1_22539006_2_0 113-143 expanded denotes substantia nigra pars compacta
SS2_22539006_2_0 145-149 abbr denotes SNpc
AE1_22539006_2_0 SS1_22539006_2_0 SS2_22539006_2_0 abbreviatedTo substantia nigra pars compacta,SNpc

UseCases_ArguminSci_Discourse

Id Subject Object Predicate Lexical cue
T3 0-221 DRI_Background denotes Twelve- to sixteen-month-old (G2019S) LRRK2 transgenic mice prepared by us displayed progressive degeneration of substantia nigra pars compacta (SNpc) dopaminergic neurons and parkinsonism phenotypes of motor dysfunction.

PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T2 0-221 DRI_Background denotes Twelve- to sixteen-month-old (G2019S) LRRK2 transgenic mice prepared by us displayed progressive degeneration of substantia nigra pars compacta (SNpc) dopaminergic neurons and parkinsonism phenotypes of motor dysfunction.

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
22539006-2#30#36#geners34637584 30-36 geners34637584 denotes G2019S
22539006-2#176#188#diseaseC0242422 176-188 diseaseC0242422 denotes parkinsonism
22539006-2#209#220#diseaseC3887505 209-220 diseaseC3887505 denotes dysfunction
30#36#geners34637584176#188#diseaseC0242422 22539006-2#30#36#geners34637584 22539006-2#176#188#diseaseC0242422 associated_with G2019S,parkinsonism
30#36#geners34637584209#220#diseaseC3887505 22539006-2#30#36#geners34637584 22539006-2#209#220#diseaseC3887505 associated_with G2019S,dysfunction

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
22539006-2#38#43#gene120892 38-43 gene120892 denotes LRRK2
22539006-2#176#188#diseaseC0242422 176-188 diseaseC0242422 denotes parkinsonism
22539006-2#209#220#diseaseC3887505 209-220 diseaseC3887505 denotes dysfunction
38#43#gene120892176#188#diseaseC0242422 22539006-2#38#43#gene120892 22539006-2#176#188#diseaseC0242422 associated_with LRRK2,parkinsonism
38#43#gene120892209#220#diseaseC3887505 22539006-2#38#43#gene120892 22539006-2#209#220#diseaseC3887505 associated_with LRRK2,dysfunction