PubMed:27930654 / 279-507 JSONTXT 16 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue db_id
11796 34-59 DiseaseOrPhenotypicFeature denotes inherited human disorders MESH:D030342
11797 61-73 DiseaseOrPhenotypicFeature denotes ciliopathies MESH:D000072661
11798 83-103 DiseaseOrPhenotypicFeature denotes retinitis pigmentosa MESH:D012174
11799 108-129 DiseaseOrPhenotypicFeature denotes Bardet-Biedl syndrome MESH:D020788
11800 131-134 DiseaseOrPhenotypicFeature denotes BBS MESH:D020788