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PubMed:17345627 JSONTXT 49 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T1 19-23 GeneOrGeneProduct denotes BMP4
T2 28-32 GeneOrGeneProduct denotes BMP5
T3 49-77 DiseaseOrPhenotypicFeature denotes axial skeletal malformations
T4 82-106 DiseaseOrPhenotypicFeature denotes heterotopic ossification
T5 124-151 GeneOrGeneProduct denotes Bone morphogenetic proteins
T6 153-157 GeneOrGeneProduct denotes BMPs
T7 223-259 DiseaseOrPhenotypicFeature denotes ectopic cartilage and bone formation
T8 296-324 GeneOrGeneProduct denotes bone morphogenetic protein 4
T9 326-330 GeneOrGeneProduct denotes BMP4
T10 357-365 OrganismTaxon denotes patients
T11 375-412 DiseaseOrPhenotypicFeature denotes fibrodysplasia ossificans progressiva
T12 414-417 DiseaseOrPhenotypicFeature denotes FOP
T13 442-486 DiseaseOrPhenotypicFeature denotes axial and appendicular skeletal malformation
T14 503-527 DiseaseOrPhenotypicFeature denotes heterotopic ossification
T15 563-591 GeneOrGeneProduct denotes bone morphogenetic protein 5
T16 593-597 GeneOrGeneProduct denotes bmp5
T17 635-639 GeneOrGeneProduct denotes BMP5
T18 650-656 OrganismTaxon denotes murine
T19 657-675 DiseaseOrPhenotypicFeature denotes short ear syndrome
T20 736-764 DiseaseOrPhenotypicFeature denotes axial skeletal malformations
T21 818-823 OrganismTaxon denotes mouse
T22 828-831 DiseaseOrPhenotypicFeature denotes FOP
T23 848-871 DiseaseOrPhenotypicFeature denotes malformed external ears
T24 873-917 DiseaseOrPhenotypicFeature denotes multiple malformations of the axial skeleton
T25 935-959 DiseaseOrPhenotypicFeature denotes heterotopic ossification
T26 994-997 GeneOrGeneProduct denotes BMP
T27 1153-1157 GeneOrGeneProduct denotes BMP4
T28 1162-1166 GeneOrGeneProduct denotes BMP5
T29 1205-1212 OrganismTaxon denotes patient
T30 1237-1241 GeneOrGeneProduct denotes BMP2
T31 1312-1316 GeneOrGeneProduct denotes BMP4
T32 1321-1325 GeneOrGeneProduct denotes BMP5
T33 1363-1368 OrganismTaxon denotes human
T34 1369-1397 DiseaseOrPhenotypicFeature denotes axial skeletal abnormalities
T35 1423-1428 OrganismTaxon denotes mouse
T36 1433-1436 DiseaseOrPhenotypicFeature denotes FOP