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PubMed:11314002 JSONTXT

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PennBioIE

Id Subject Object Predicate Lexical cue
T1 0-22 protein denotes Loss of heterozygosity
T2 26-32 protein denotes 4p16.3
T3 49-54 protein denotes FGFR3
T4 87-93 protein denotes 4p16.3
T5 151-154 protein denotes LOH
T6 216-238 protein denotes tumour suppressor gene
T7 276-311 protein denotes fibroblast growth factor receptor 3
T8 313-318 protein denotes FGFR3
T9 343-348 protein denotes FGFR3
T10 492-503 protein denotes the protein
T11 549-554 protein denotes FGFR3
T12 674-696 protein denotes loss of heterozygosity
T13 698-701 protein denotes LOH
T14 706-712 protein denotes 4p16.3
T15 714-719 protein denotes FGFR3
T16 1025-1028 protein denotes LOH
T17 1032-1038 protein denotes 4p16.3
T18 1112-1130 protein denotes missense mutations
T19 1134-1139 protein denotes FGFR3
T20 1283-1284 protein denotes K
T21 1284-1287 protein denotes 652
T22 1287-1288 protein denotes Q
T23 1393-1396 protein denotes LOH
T24 1400-1406 protein denotes 4p16.3
T25 1424-1429 protein denotes FGFR3
T26 1505-1510 protein denotes FGFR3
T27 1535-1547 protein denotes this protein

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
11314002-10#21#26#geners78311289 1283-1288 geners78311289 denotes K652Q
11314002-10#86#104#diseaseC0029422 1348-1366 diseaseC0029422 denotes skeletal dysplasia
11314002-10#86#104#diseaseC0410528 1348-1366 diseaseC0410528 denotes skeletal dysplasia
21#26#geners7831128986#104#diseaseC0029422 11314002-10#21#26#geners78311289 11314002-10#86#104#diseaseC0029422 associated_with K652Q,skeletal dysplasia
21#26#geners7831128986#104#diseaseC0410528 11314002-10#21#26#geners78311289 11314002-10#86#104#diseaseC0410528 associated_with K652Q,skeletal dysplasia

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
11314002-0#49#54#gene2261 49-54 gene2261 denotes FGFR3
11314002-0#58#85#diseaseC0007138 58-85 diseaseC0007138 denotes transitional cell carcinoma
11314002-12#17#22#gene2261 1505-1510 gene2261 denotes FGFR3
11314002-12#87#90#diseaseC1861305 1575-1578 diseaseC1861305 denotes TCC
49#54#gene226158#85#diseaseC0007138 11314002-0#49#54#gene2261 11314002-0#58#85#diseaseC0007138 associated_with FGFR3,transitional cell carcinoma
17#22#gene226187#90#diseaseC1861305 11314002-12#17#22#gene2261 11314002-12#87#90#diseaseC1861305 associated_with FGFR3,TCC

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1505-1510 gene:2261 denotes FGFR3
T1 1575-1578 disease:C0007138 denotes TCC
R1 T0 T1 associated_with FGFR3,TCC