> top > docs > PubMed:10090890 > annotations

PubMed:10090890 JSONTXT

Annnotations TAB JSON ListView MergeView

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 23-38 DiseaseOrPhenotypicFeature denotes hemochromatosis 0006507
T2 69-84 DiseaseOrPhenotypicFeature denotes hemochromatosis 0006507
T3 1460-1470 DiseaseOrPhenotypicFeature denotes infectious 0005550
T4 1516-1533 DiseaseOrPhenotypicFeature denotes genetic disorders 0003847
T5 1542-1548 DiseaseOrPhenotypicFeature denotes anemia 0002280

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 23-38 Modifier:D006432 denotes hemochromatosis
T2 61-84 SpecificDisease:D006432 denotes Genetic hemochromatosis
T3 86-88 SpecificDisease:D006432 denotes GH
T4 192-194 Modifier:D006432 denotes GH
T5 350-352 Modifier:D006432 denotes GH
T6 1460-1479 DiseaseClass:D003141 denotes infectious diseases
T7 1516-1533 DiseaseClass:D030342 denotes genetic disorders
T8 1542-1548 DiseaseClass:D000740 denotes anemia

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 1542-1548 HP_0001903 denotes anemia

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T1370 23-38 Modifier denotes hemochromatosis D006432
T1371 61-84 SpecificDisease denotes Genetic hemochromatosis D006432
T1372 86-88 SpecificDisease denotes GH D006432
T1373 192-194 Modifier denotes GH D006432
T1374 350-352 Modifier denotes GH D006432
T1375 1460-1479 DiseaseClass denotes infectious diseases D003141
T1376 1516-1533 DiseaseClass denotes genetic disorders D030342
T1377 1542-1548 DiseaseClass denotes anemia D000740

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T1370 23-38 Modifier denotes hemochromatosis D006432
T1371 61-84 SpecificDisease denotes Genetic hemochromatosis D006432
T1372 86-88 SpecificDisease denotes GH D006432
T1373 192-194 Modifier denotes GH D006432
T1374 350-352 Modifier denotes GH D006432
T1375 1460-1479 DiseaseClass denotes infectious diseases D003141
T1376 1516-1533 DiseaseClass denotes genetic disorders D030342
T1377 1542-1548 DiseaseClass denotes anemia D000740

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 23-38 Modifier denotes hemochromatosis
T2 69-84 SpecificDisease denotes hemochromatosis
T3 192-194 Modifier denotes GH
T4 350-352 Modifier denotes GH
T5 1471-1479 DiseaseClass denotes diseases
T6 1542-1548 DiseaseClass denotes anemia

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 23-38 Modifier denotes hemochromatosis
T2 69-84 SpecificDisease denotes hemochromatosis
T3 192-194 Modifier denotes GH
T4 350-352 Modifier denotes GH
T5 1365-1368 Modifier denotes HFE
T6 1471-1479 DiseaseClass denotes diseases
T7 1542-1548 DiseaseClass denotes anemia

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 23-38 SpecificDisease denotes hemochromatosis
T2 61-84 SpecificDisease denotes Genetic hemochromatosis
T3 192-194 Modifier denotes GH
T4 350-352 Modifier denotes GH
T5 1542-1548 SpecificDisease denotes anemia

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 23-38 SpecificDisease denotes hemochromatosis
T2 61-89 SpecificDisease denotes Genetic hemochromatosis (GH)
T3 192-194 SpecificDisease denotes GH
T4 350-352 SpecificDisease denotes GH
T5 1460-1479 DiseaseClass denotes infectious diseases
T6 1542-1548 SpecificDisease denotes anemia