PubMed:2303461 / 408-411 JSONTXT

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    DisGeNET

    {"project":"DisGeNET","denotations":[{"id":"T1","span":{"begin":0,"end":3},"obj":"disease:C0520463"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"CAH"}

    DisGeNET5_gene_disease

    {"project":"DisGeNET5_gene_disease","denotations":[{"id":"2303461-3#98#101#diseaseC0520463","span":{"begin":0,"end":3},"obj":"diseaseC0520463"}],"text":"CAH"}

    mondo_disease

    {"project":"mondo_disease","denotations":[{"id":"T9","span":{"begin":0,"end":3},"obj":"Disease"}],"attributes":[{"id":"A9","pred":"mondo_id","subj":"T9","obj":"http://purl.obolibrary.org/obo/MONDO_0018479"},{"id":"A10","pred":"mondo_id","subj":"T9","obj":"http://purl.obolibrary.org/obo/MONDO_0015898"}],"text":"CAH"}

    HP-phenotype

    {"project":"HP-phenotype","denotations":[{"id":"T4","span":{"begin":0,"end":3},"obj":"Phenotype"}],"attributes":[{"id":"A4","pred":"hp_id","subj":"T4","obj":"HP:0008258"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}],"text":"CAH"}