PubMed:15749661 JSONTXT 28 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label ID:
T25393 21-26 SequenceVariant denotes L490R
T21389 31-36 SequenceVariant denotes V561X
T2016 45-67 GeneOrGeneProduct denotes transferrin receptor 2
T51052 85-93 OrganismTaxon denotes patients
T55300 99-114 DiseaseOrPhenotypicFeature denotes hemochromatosis D006432
T25728 169-174 SequenceVariant denotes C282Y
T52898 246-261 DiseaseOrPhenotypicFeature denotes hemochromatosis D006432
T25154 274-282 OrganismTaxon denotes patients
T40430 339-347 OrganismTaxon denotes patients
T56457 384-399 SequenceVariant denotes deletion of the
T2 400-420 GeneOrGeneProduct denotes transferrin receptor
T97309 482-497 DiseaseOrPhenotypicFeature denotes hemochromatosis D006432
T50389 510-518 OrganismTaxon denotes patients
T30199 545-553 OrganismTaxon denotes patients
T4 580-595 DiseaseOrPhenotypicFeature denotes hemochromatosis D006432
T82976 851-858 GeneOrGeneProduct denotes gene, 2
T91771 876-881 SequenceVariant denotes 1469T
T86180 886-891 SequenceVariant denotes L490R
T35022 897-905 SequenceVariant denotes 1665delC
T23684 907-912 SequenceVariant denotes V561X
T56613 931-939 OrganismTaxon denotes patients
T86165 960-964 SequenceVariant denotes 714C
T92726 968-973 SequenceVariant denotes I238M
T82401 998-1005 OrganismTaxon denotes patient
T1932 1011-1016 SequenceVariant denotes L490R
T6192 1022-1029 OrganismTaxon denotes patient
T56720 1050-1055 SequenceVariant denotes L490R
T24456 1060-1065 SequenceVariant denotes I238M
T5 1105-1120 DiseaseOrPhenotypicFeature denotes hemochromatosis D006432
T23640 1159-1168 DiseaseOrPhenotypicFeature denotes cirrhotic DISEASE
T1 1186-1190 ChemicalEntity denotes iron http://purl.obolibrary.org/obo/CHEBI_18248|D007501
T3 1220-1227 ChemicalEntity denotes glucose http://purl.obolibrary.org/obo/CHEBI_17234|http://purl.obolibrary.org/obo/CHEBI_4167|D005947
T7 1263-1280 DiseaseOrPhenotypicFeature denotes diabetes mellitus D003920
T72565 1286-1293 OrganismTaxon denotes patient
T14 1309-1314 SequenceVariant denotes V561X
T6 1326-1330 ChemicalEntity denotes iron http://purl.obolibrary.org/obo/CHEBI_18248|D007501
T8 1326-1339 DiseaseOrPhenotypicFeature denotes iron overload D019190
T9 1358-1367 DiseaseOrPhenotypicFeature denotes cirrhosis D005355
T10 1369-1386 DiseaseOrPhenotypicFeature denotes diabetes mellitus D003920
T11 1391-1408 DiseaseOrPhenotypicFeature denotes skin pigmentation DISEASE
T99738 1518-1526 OrganismTaxon denotes patients
T12 1532-1547 DiseaseOrPhenotypicFeature denotes hemochromatosis D006432
T13 1653-1668 DiseaseOrPhenotypicFeature denotes hemochromatosis D006432