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PubMed:15041272 JSONTXT 19 Projects

Annnotations TAB TSV DIC JSON TextAE-old TextAE

Id Subject Object Predicate Lexical cue #label ID:
T1 36-66 DiseaseOrPhenotypicFeature denotes type 2B von Willebrand disease D056728
T46254 72-78 SequenceVariant denotes R1306W
T2 114-128 DiseaseOrPhenotypicFeature denotes genetic defect DISEASE
T3 156-186 DiseaseOrPhenotypicFeature denotes type 2B von Willebrand disease D056728
T4 188-191 DiseaseOrPhenotypicFeature denotes VWD D014842
T30794 233-242 OrganismTaxon denotes old woman
T5 352-361 DiseaseOrPhenotypicFeature denotes bleedings D006470
T24079 401-404 ChemicalEntity denotes PTT http://purl.obolibrary.org/obo/CHEBI_3088
T50816 409-423 GeneOrGeneProduct denotes platelet count
T6 446-454 DiseaseOrPhenotypicFeature denotes bleeding D006470
T77624 488-509 GeneOrGeneProduct denotes von Willebrand factor
T38787 557-567 ChemicalEntity denotes ristocetin http://purl.obolibrary.org/obo/CHEBI_85129
T27974 593-603 ChemicalEntity denotes ristocetin http://purl.obolibrary.org/obo/CHEBI_85129
T4499 634-638 GeneOrGeneProduct denotes RIPA
T50705 664-674 ChemicalEntity denotes ristocetin http://purl.obolibrary.org/obo/CHEBI_85129
T65281 731-741 ChemicalEntity denotes ristocetin http://purl.obolibrary.org/obo/CHEBI_85129
T53768 829-850 GeneOrGeneProduct denotes von Willebrand factor
T94915 852-855 GeneOrGeneProduct denotes VWF
T79085 1016-1019 GeneOrGeneProduct denotes VWF
T4122 1211-1214 ChemicalEntity denotes Arg http://purl.obolibrary.org/obo/CHEBI_29952|http://purl.obolibrary.org/obo/CHEBI_16467
T82792 1211-1223 SequenceVariant denotes Arg 1306 Trp
T14858 1220-1223 ChemicalEntity denotes Trp http://purl.obolibrary.org/obo/CHEBI_29954|http://purl.obolibrary.org/obo/CHEBI_27897|http://purl.obolibrary.org/obo/CHEBI_16828
T92092 1225-1231 SequenceVariant denotes R1306W
T6501 1268-1280 GeneOrGeneProduct denotes glycoprotein
T4501 1354-1357 GeneOrGeneProduct denotes VWF
T7 1420-1436 DiseaseOrPhenotypicFeature denotes thrombocytopenia D013921
T8 1479-1482 DiseaseOrPhenotypicFeature denotes VWD D014842
T57553 1522-1528 SequenceVariant denotes R1306W
T9 1541-1544 GeneOrGeneProduct denotes VWF