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PubMed:10802668 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 105-123 HP_0000006 denotes autosomal dominant
T2 159-173 HP_0003202 denotes muscle wasting
T3 175-183 HP_0002486 denotes myotonia
T4 185-203 HP_0011675 denotes cardiac arrhythmia
T5 193-203 HP_0011675 denotes arrhythmia
T6 224-242 HP_0001249 denotes mental retardation
T7 254-263 HP_0000518 denotes cataracts
T8 1081-1109 HP_0011675 denotes cardiac conduction disorders
T9 1263-1271 HP_0000518 denotes cataract
T10 1542-1550 HP_0000518 denotes cataract
T11 1572-1581 HP_0000518 denotes cataracts
T12 1760-1784 HP_0001466 denotes contiguous gene syndrome

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 64-73 SpecificDisease:D002386 denotes cataracts
T2 75-93 SpecificDisease:D009223 denotes Myotonic dystrophy
T3 95-97 SpecificDisease:D009223 denotes DM
T4 105-131 DiseaseClass:D030342 denotes autosomal dominant disorde
T5 159-173 SpecificDisease:D009133 denotes muscle wasting
T6 175-183 DiseaseClass:D009222 denotes myotonia
T7 185-203 DiseaseClass:D001145 denotes cardiac arrhythmia
T8 205-222 SpecificDisease:D006946 denotes hyperinsulinaemia
T9 224-242 DiseaseClass:D008607 denotes mental retardation
T10 254-263 SpecificDisease:D002386 denotes cataracts
T11 269-283 DiseaseClass:D030342 denotes genetic defect
T12 287-289 SpecificDisease:D009223 denotes DM
T13 498-500 SpecificDisease:D009223 denotes DM
T14 1000-1002 Modifier:D009223 denotes DM
T15 1081-1109 DiseaseClass:D001145 denotes cardiac conduction disorders
T16 1144-1146 SpecificDisease:D009223 denotes DM
T17 1263-1271 Modifier:D002386 denotes cataract
T18 1542-1550 Modifier:D002386 denotes cataract
T19 1572-1581 SpecificDisease:D002386 denotes cataracts
T20 1614-1616 SpecificDisease:D009223 denotes DM
T21 1711-1713 SpecificDisease:D009223 denotes DM
T22 1752-1754 SpecificDisease:D009223 denotes DM

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T1646 64-73 SpecificDisease denotes cataracts D002386
T1647 75-93 SpecificDisease denotes Myotonic dystrophy D009223
T1648 95-97 SpecificDisease denotes DM D009223
T1649 105-131 DiseaseClass denotes autosomal dominant disorde D030342
T1650 159-173 SpecificDisease denotes muscle wasting D009133
T1651 175-183 DiseaseClass denotes myotonia D009222
T1652 185-203 DiseaseClass denotes cardiac arrhythmia D001145
T1653 205-222 SpecificDisease denotes hyperinsulinaemia D006946
T1654 224-242 DiseaseClass denotes mental retardation D008607
T1655 254-263 SpecificDisease denotes cataracts D002386
T1656 269-283 DiseaseClass denotes genetic defect D030342
T1657 287-289 SpecificDisease denotes DM D009223
T1658 498-500 SpecificDisease denotes DM D009223
T1659 1000-1002 Modifier denotes DM D009223
T1660 1081-1109 DiseaseClass denotes cardiac conduction disorders D001145
T1661 1144-1146 SpecificDisease denotes DM D009223
T1662 1263-1271 Modifier denotes cataract D002386
T1663 1542-1550 Modifier denotes cataract D002386
T1664 1572-1581 SpecificDisease denotes cataracts D002386
T1665 1614-1616 SpecificDisease denotes DM D009223
T1666 1711-1713 SpecificDisease denotes DM D009223
T1667 1752-1754 SpecificDisease denotes DM D009223

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T1646 64-73 SpecificDisease denotes cataracts D002386
T1647 75-93 SpecificDisease denotes Myotonic dystrophy D009223
T1648 95-97 SpecificDisease denotes DM D009223
T1649 105-131 DiseaseClass denotes autosomal dominant disorde D030342
T1650 159-173 SpecificDisease denotes muscle wasting D009133
T1651 175-183 DiseaseClass denotes myotonia D009222
T1652 185-203 DiseaseClass denotes cardiac arrhythmia D001145
T1653 205-222 SpecificDisease denotes hyperinsulinaemia D006946
T1654 224-242 DiseaseClass denotes mental retardation D008607
T1655 254-263 SpecificDisease denotes cataracts D002386
T1656 269-283 DiseaseClass denotes genetic defect D030342
T1657 287-289 SpecificDisease denotes DM D009223
T1658 498-500 SpecificDisease denotes DM D009223
T1659 1000-1002 Modifier denotes DM D009223
T1660 1081-1109 DiseaseClass denotes cardiac conduction disorders D001145
T1661 1144-1146 SpecificDisease denotes DM D009223
T1662 1263-1271 Modifier denotes cataract D002386
T1663 1542-1550 Modifier denotes cataract D002386
T1664 1572-1581 SpecificDisease denotes cataracts D002386
T1665 1614-1616 SpecificDisease denotes DM D009223
T1666 1711-1713 SpecificDisease denotes DM D009223
T1667 1752-1754 SpecificDisease denotes DM D009223

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 64-73 SpecificDisease denotes cataracts
T2 75-93 SpecificDisease denotes Myotonic dystrophy
T3 95-97 SpecificDisease denotes DM
T4 254-263 SpecificDisease denotes cataracts
T5 287-289 SpecificDisease denotes DM
T6 498-500 SpecificDisease denotes DM
T7 1000-1002 SpecificDisease denotes DM
T8 1144-1146 SpecificDisease denotes DM
T9 1263-1281 SpecificDisease denotes cataract formation
T10 1542-1560 SpecificDisease denotes cataract formation
T11 1572-1581 SpecificDisease denotes cataracts
T12 1614-1616 SpecificDisease denotes DM
T13 1711-1713 SpecificDisease denotes DM
T14 1752-1754 SpecificDisease denotes DM

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 64-73 SpecificDisease denotes cataracts
T2 75-93 SpecificDisease denotes Myotonic dystrophy
T3 95-97 SpecificDisease denotes DM
T4 175-183 SpecificDisease denotes myotonia
T5 193-203 SpecificDisease denotes arrhythmia
T6 254-263 SpecificDisease denotes cataracts
T7 287-289 SpecificDisease denotes DM
T8 498-500 SpecificDisease denotes DM
T9 1000-1002 SpecificDisease denotes DM
T10 1144-1146 SpecificDisease denotes DM
T11 1263-1271 SpecificDisease denotes cataract
T12 1542-1550 SpecificDisease denotes cataract
T13 1572-1581 SpecificDisease denotes cataracts
T14 1614-1616 SpecificDisease denotes DM
T15 1711-1713 SpecificDisease denotes DM
T16 1752-1754 SpecificDisease denotes DM

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 57-73 SpecificDisease denotes ocular cataracts
T2 75-93 SpecificDisease denotes Myotonic dystrophy
T3 105-132 DiseaseClass denotes autosomal dominant disorder
T4 247-263 SpecificDisease denotes ocular cataracts
T5 287-289 SpecificDisease denotes DM
T6 498-500 SpecificDisease denotes DM
T7 1000-1002 SpecificDisease denotes DM
T8 1100-1109 DiseaseClass denotes disorders
T9 1144-1146 SpecificDisease denotes DM
T10 1263-1281 SpecificDisease denotes cataract formation
T11 1542-1560 SpecificDisease denotes cataract formation
T12 1565-1581 SpecificDisease denotes ocular cataracts
T13 1614-1616 SpecificDisease denotes DM
T14 1711-1713 SpecificDisease denotes DM
T15 1752-1754 SpecificDisease denotes DM

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 64-73 SpecificDisease denotes cataracts
T2 75-93 SpecificDisease denotes Myotonic dystrophy
T3 124-132 SpecificDisease denotes disorder
T4 254-263 SpecificDisease denotes cataracts
T5 1100-1109 SpecificDisease denotes disorders
T6 1263-1281 SpecificDisease denotes cataract formation
T7 1542-1560 SpecificDisease denotes cataract formation
T8 1572-1581 SpecificDisease denotes cataracts