PubMed:18412970 / 0-284
Annnotations
c_corpus
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PMID_GLOBAL
{"project":"PMID_GLOBAL","denotations":[{"id":"T1","span":{"begin":212,"end":232},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":234,"end":236},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0007739"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0007739"}],"text":"Elucidating a normal function of huntingtin by functional and microarray analysis of huntingtin-null mouse embryonic fibroblasts.\nBACKGROUND: The polyglutamine expansion in huntingtin (Htt) protein is a cause of Huntington's disease (HD). Htt is an essential gene as deletion of the m"}
UseCases_ArguminSci_Discourse
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