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PubMed:17392156 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 25-27 DiseaseOrPhenotypicFeature denotes CC 0019087
T2 41-43 DiseaseOrPhenotypicFeature denotes CC 0019087
T3 75-93 DiseaseOrPhenotypicFeature denotes pulmonary fibrosis 0002771
T4 183-217 DiseaseOrPhenotypicFeature denotes Idiopathic interstitial pneumonias 0002429
T5 219-223 DiseaseOrPhenotypicFeature denotes IIPs 0002429
T6 302-304 DiseaseOrPhenotypicFeature denotes CC 0019087
T7 408-426 DiseaseOrPhenotypicFeature denotes pulmonary fibrosis 0002771
T8 510-528 DiseaseOrPhenotypicFeature denotes pulmonary fibrosis 0002771
T9 573-602 DiseaseOrPhenotypicFeature denotes idiopathic pulmonary fibrosis 0008345
T10 603-631 DiseaseOrPhenotypicFeature denotes usual interstitial pneumonia 0008345
T11 633-667 DiseaseOrPhenotypicFeature denotes nonspecific interstitial pneumonia 0019622
T12 743-775 DiseaseOrPhenotypicFeature denotes severe combined immunodeficiency 0015974
T13 777-781 DiseaseOrPhenotypicFeature denotes SCID 0015974
T14 824-853 DiseaseOrPhenotypicFeature denotes idiopathic pulmonary fibrosis 0008345
T15 854-882 DiseaseOrPhenotypicFeature denotes usual interstitial pneumonia 0008345
T16 1037-1071 DiseaseOrPhenotypicFeature denotes nonspecific interstitial pneumonia 0019622
T17 1353-1355 DiseaseOrPhenotypicFeature denotes CC 0019087
T18 1408-1426 DiseaseOrPhenotypicFeature denotes pulmonary fibrosis 0002771
T19 1547-1565 DiseaseOrPhenotypicFeature denotes pulmonary fibrosis 0002771
T20 1739-1741 DiseaseOrPhenotypicFeature denotes CC 0019087

DisGeNET

Id Subject Object Predicate Lexical cue
T0 41-64 gene:1236 denotes CC chemokine receptor 7
T1 75-93 disease:C0034069 denotes pulmonary fibrosis
T2 41-64 gene:1236 denotes CC chemokine receptor 7
T3 161-176 disease:C0021051 denotes immunodeficient
R1 T0 T1 associated_with CC chemokine receptor 7,pulmonary fibrosis
R2 T2 T3 associated_with CC chemokine receptor 7,immunodeficient

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 207-217 HP_0002090 denotes pneumonias
T2 408-426 HP_0002206 denotes pulmonary fibrosis
T3 510-528 HP_0002206 denotes pulmonary fibrosis
T4 584-602 HP_0002206 denotes pulmonary fibrosis
T5 622-631 HP_0002090 denotes pneumonia
T6 658-667 HP_0002090 denotes pneumonia
T7 743-775 HP_0004430 denotes severe combined immunodeficiency
T8 750-775 HP_0005387 denotes combined immunodeficiency
T9 759-775 HP_0002721 denotes immunodeficiency
T10 835-853 HP_0002206 denotes pulmonary fibrosis
T11 873-882 HP_0002090 denotes pneumonia
T12 992-1007 HP_0002721 denotes immunodeficient
T13 1062-1071 HP_0002090 denotes pneumonia
T14 1408-1426 HP_0002206 denotes pulmonary fibrosis
T15 1547-1565 HP_0002206 denotes pulmonary fibrosis
T16 1650-1665 HP_0002721 denotes immunodeficient

Ab3P-abbreviations

Id Subject Object Predicate Lexical cue
SF0 219-223 ABBR denotes IIPs
LF0 183-217 ABBR denotes Idiopathic interstitial pneumonias
SF1 327-331 ABBR denotes CCR7
LF1 302-325 ABBR denotes CC chemokine receptor 7
SF2 777-781 ABBR denotes SCID
LF2 743-775 ABBR denotes severe combined immunodeficiency
SF3 790-792 ABBR denotes bg
LF3 783-788 ABBR denotes beige
R0 LF0 SF0 ShortForm Idiopathic interstitial pneumonias,IIPs
R1 LF1 SF1 ShortForm CC chemokine receptor 7,CCR7
R2 LF2 SF2 ShortForm severe combined immunodeficiency,SCID
R3 LF3 SF3 ShortForm beige,bg

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
17392156-0#41#64#gene1236 41-64 gene1236 denotes CC chemokine receptor 7
17392156-0#75#93#diseaseC0034069 75-93 diseaseC0034069 denotes pulmonary fibrosis
17392156-0#161#176#diseaseC0021051 161-176 diseaseC0021051 denotes immunodeficient
41#64#gene123675#93#diseaseC0034069 17392156-0#41#64#gene1236 17392156-0#75#93#diseaseC0034069 associated_with CC chemokine receptor 7,pulmonary fibrosis
41#64#gene1236161#176#diseaseC0021051 17392156-0#41#64#gene1236 17392156-0#161#176#diseaseC0021051 associated_with CC chemokine receptor 7,immunodeficient