PubMed:2303461 / 0-146 JSONTXT

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    sentences

    {"project":"sentences","denotations":[{"id":"T1","span":{"begin":0,"end":95},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":95},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.\nCongenital adrenal hyperplasia (CAH) is a common r"}

    PubmedHPO

    {"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":96,"end":126},"obj":"HP_0008258"},{"id":"T2","span":{"begin":107,"end":126},"obj":"HP_0008221"}],"text":"A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.\nCongenital adrenal hyperplasia (CAH) is a common r"}

    DisGeNET5_variant_disease

    {"project":"DisGeNET5_variant_disease","denotations":[{"id":"2303461-0#23#36#geners6475","span":{"begin":23,"end":36},"obj":"geners6475"},{"id":"2303461-0#40#53#geners7769409","span":{"begin":40,"end":53},"obj":"geners7769409"},{"id":"2303461-0#61#94#diseaseC0268287","span":{"begin":61,"end":94},"obj":"diseaseC0268287"}],"relations":[{"id":"23#36#geners647561#94#diseaseC0268287","pred":"associated_with","subj":"2303461-0#23#36#geners6475","obj":"2303461-0#61#94#diseaseC0268287"},{"id":"40#53#geners776940961#94#diseaseC0268287","pred":"associated_with","subj":"2303461-0#40#53#geners7769409","obj":"2303461-0#61#94#diseaseC0268287"}],"text":"A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.\nCongenital adrenal hyperplasia (CAH) is a common r"}

    DisGeNET5_gene_disease

    {"project":"DisGeNET5_gene_disease","denotations":[{"id":"2303461-1#0#30#diseaseC0001627","span":{"begin":96,"end":126},"obj":"diseaseC0001627"}],"text":"A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.\nCongenital adrenal hyperplasia (CAH) is a common r"}

    PubCasesHPO

    {"project":"PubCasesHPO","denotations":[{"id":"AB1","span":{"begin":96,"end":126},"obj":"HP:0008258"}],"text":"A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.\nCongenital adrenal hyperplasia (CAH) is a common r"}

    mondo_disease

    {"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":69,"end":94},"obj":"Disease"},{"id":"T2","span":{"begin":96,"end":126},"obj":"Disease"},{"id":"T3","span":{"begin":107,"end":126},"obj":"Disease"},{"id":"T4","span":{"begin":128,"end":131},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0008728"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0015898"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MONDO_0018479"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/MONDO_0018479"},{"id":"A5","pred":"mondo_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/MONDO_0015898"}],"text":"A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.\nCongenital adrenal hyperplasia (CAH) is a common r"}

    Anatomy-UBERON

    {"project":"Anatomy-UBERON","denotations":[{"id":"T1","span":{"begin":107,"end":114},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"uberon_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/UBERON_0002369"}],"text":"A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.\nCongenital adrenal hyperplasia (CAH) is a common r"}

    HP-phenotype

    {"project":"HP-phenotype","denotations":[{"id":"T1","span":{"begin":96,"end":126},"obj":"Phenotype"},{"id":"T2","span":{"begin":128,"end":131},"obj":"Phenotype"}],"attributes":[{"id":"A1","pred":"hp_id","subj":"T1","obj":"HP:0008258"},{"id":"A2","pred":"hp_id","subj":"T2","obj":"HP:0008258"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}],"text":"A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.\nCongenital adrenal hyperplasia (CAH) is a common r"}