PubMed:10102532 / 74-234 JSONTXT

{"project":"PMID_GLOBAL","denotations":[{"id":"T3","span":{"begin":46,"end":68},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":70,"end":73},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0019565"},{"id":"A4","pred":"mondo_id","subj":"T3","obj":"0024574"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0019565"}],"text":"A 10-year-old male patient affected by type 2 von Willebrand disease (vWD) and his family members were investigated by hemostatic and molecular genetic studies."}

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{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":46,"end":68},"obj":"ORDO:903"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"A 10-year-old male patient affected by type 2 von Willebrand disease (vWD) and his family members were investigated by hemostatic and molecular genetic studies."}