PubMed:8376405 / 0-190 JSONTXT

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    sentences

    {"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":133},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":133},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Type IIB mutation His-505--\u003eAsp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib.\nType IIB von Willebrand disease is characterized by incr"}

    PubCasesORDO

    {"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":143,"end":165},"obj":"ORDO:903"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Type IIB mutation His-505--\u003eAsp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib.\nType IIB von Willebrand disease is characterized by incr"}

    mondo_disease

    {"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":143,"end":165},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0019565"},{"id":"A2","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0024574"}],"text":"Type IIB mutation His-505--\u003eAsp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib.\nType IIB von Willebrand disease is characterized by incr"}

    Anatomy-UBERON

    {"project":"Anatomy-UBERON","denotations":[{"id":"T1","span":{"begin":49,"end":56},"obj":"Body_part"},{"id":"T2","span":{"begin":108,"end":116},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"uberon_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/UBERON_0000914"},{"id":"A2","pred":"uberon_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/CL_0000233"}],"text":"Type IIB mutation His-505--\u003eAsp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib.\nType IIB von Willebrand disease is characterized by incr"}

    CL-cell

    {"project":"CL-cell","denotations":[{"id":"T1","span":{"begin":108,"end":116},"obj":"Cell"}],"attributes":[{"id":"A1","pred":"cl_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/CL:0000233"}],"text":"Type IIB mutation His-505--\u003eAsp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib.\nType IIB von Willebrand disease is characterized by incr"}