CORD-19:12af471f81b05440047e30b963b3733bd6f33693 / 50213-50313 JSONTXT

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    CORD-19_Custom_license_subset

    {"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T13","span":{"begin":0,"end":100},"obj":"Sentence"}],"text":"The primary disease genome G is the set of molecular anomalies that are associated to the phenotype."}

    CORD-19-Sentences

    {"project":"CORD-19-Sentences","denotations":[{"id":"T1070","span":{"begin":0,"end":100},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"The primary disease genome G is the set of molecular anomalies that are associated to the phenotype."}

    Epistemic_Statements

    {"project":"Epistemic_Statements","denotations":[{"id":"T136","span":{"begin":0,"end":100},"obj":"Epistemic_statement"}],"text":"The primary disease genome G is the set of molecular anomalies that are associated to the phenotype."}