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PubMed:15958417 / 320-492 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T4 0-172 Sentence denotes Other genes (POMT1, POMGnT1, fukutin, and FKRP) that encode known or putative glycosylation enzymes are also causally associated with human congenital muscular dystrophies.
T3 0-172 Sentence denotes Other genes (POMT1, POMGnT1, fukutin, and FKRP) that encode known or putative glycosylation enzymes are also causally associated with human congenital muscular dystrophies.
T4 0-172 Sentence denotes Other genes (POMT1, POMGnT1, fukutin, and FKRP) that encode known or putative glycosylation enzymes are also causally associated with human congenital muscular dystrophies.

GlycoBiology-GDGDB

Id Subject Object Predicate Lexical cue
_T3 13-18 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00376 denotes POMT1
_T4 20-27 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00377 denotes POMGnT1
_T5 42-46 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00382 denotes FKRP
_T6 42-46 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00381 denotes FKRP
_T14 140-171 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 denotes congenital muscular dystrophies
_T15 140-171 http://acgg.asia/db/diseases/gdgdb?con_ui=CON00381 denotes congenital muscular dystrophies

ICD10

Id Subject Object Predicate Lexical cue
T2 151-171 http://purl.bioontology.org/ontology/ICD10/G71.0 denotes muscular dystrophies

uniprot-human

Id Subject Object Predicate Lexical cue
T10 13-18 http://www.uniprot.org/uniprot/Q9NX32 denotes POMT1
T11 20-27 http://www.uniprot.org/uniprot/Q8WZA1 denotes POMGnT1
T12 29-36 http://www.uniprot.org/uniprot/O75072 denotes fukutin
T13 42-46 http://www.uniprot.org/uniprot/Q9H9S5 denotes FKRP

uniprot-mouse

Id Subject Object Predicate Lexical cue
T1 20-27 http://www.uniprot.org/uniprot/Q91X88 denotes POMGnT1
T2 29-36 http://www.uniprot.org/uniprot/Q8R507 denotes fukutin

GO-BP

Id Subject Object Predicate Lexical cue
T1 78-91 http://purl.obolibrary.org/obo/GO_0070085 denotes glycosylation

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
15958417-3#29#36#gene2218 29-36 gene2218 denotes fukutin
15958417-3#42#46#gene79147 42-46 gene79147 denotes FKRP
15958417-3#151#171#diseaseC0026850 151-171 diseaseC0026850 denotes muscular dystrophies
29#36#gene2218151#171#diseaseC0026850 15958417-3#29#36#gene2218 15958417-3#151#171#diseaseC0026850 associated_with fukutin,muscular dystrophies
42#46#gene79147151#171#diseaseC0026850 15958417-3#42#46#gene79147 15958417-3#151#171#diseaseC0026850 associated_with FKRP,muscular dystrophies

DisGeNET

Id Subject Object Predicate Lexical cue
T0 29-36 gene:2218 denotes fukutin
T1 151-171 disease:C0026850 denotes muscular dystrophies
T2 42-46 gene:79147 denotes FKRP
T3 151-171 disease:C0026850 denotes muscular dystrophies
R1 T0 T1 associated_with fukutin,muscular dystrophies
R2 T2 T3 associated_with FKRP,muscular dystrophies

HP-phenotype

Id Subject Object Predicate Lexical cue hp_id
T2 140-171 Phenotype denotes congenital muscular dystrophies HP:0003560

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T4 140-171 Disease denotes congenital muscular dystrophies http://purl.obolibrary.org/obo/MONDO_0019950

NCBITAXON

Id Subject Object Predicate Lexical cue db_id
T4 134-139 OrganismTaxon denotes human 9606