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PubMed:12007509 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-90 Sentence denotes A case of smouldering mastocytosis with peripheral blood eosinophilia and lymphadenopathy.
TextSentencer_T2 91-262 Sentence denotes Systemic mastocytosis (SM) is a clonal hematologic disease showing abnormal growth and accumulation of mast cells (MC) in visceral organs with or without skin involvement.
TextSentencer_T3 263-301 Sentence denotes The clinical course in SM is variable.
TextSentencer_T4 302-364 Sentence denotes In fact, indolent and aggressive variants have been described.
TextSentencer_T5 365-466 Sentence denotes In addition, SM patients may acquire an associated hematologic clonal non-MC lineage disease (AHNMD).
TextSentencer_T6 467-602 Sentence denotes In some cases, hematologic parameters are indicative of slowly progressing SM although the clinical course remains indolent over years.
TextSentencer_T7 603-655 Sentence denotes These cases have been referred to as smouldering SM.
TextSentencer_T8 656-891 Sentence denotes We report on a smouldering patient presenting with typical skin lesions, hypercellular marrow with focal MC aggregates, persistent leukocytosis (20,000-30,000/microl) with eosinophilia (5-10%), marked lymphadenopathy, and splenomegaly.
TextSentencer_T9 892-953 Sentence denotes The C-KIT mutation Asp-816-Val confirmed the diagnosis of SM.
TextSentencer_T10 954-1100 Sentence denotes The clinical picture remained stable during an observation period of 10 years without signs of progression to an AHNMD or a high grade MC disease.
TextSentencer_T11 1101-1275 Sentence denotes These data show that some patients with SM can remain in a clinically indolent smouldering state over years even when presenting with marked eosinophilia and lymphadenopathy.
T1 0-90 Sentence denotes A case of smouldering mastocytosis with peripheral blood eosinophilia and lymphadenopathy.
T2 91-262 Sentence denotes Systemic mastocytosis (SM) is a clonal hematologic disease showing abnormal growth and accumulation of mast cells (MC) in visceral organs with or without skin involvement.
T3 263-301 Sentence denotes The clinical course in SM is variable.
T4 302-364 Sentence denotes In fact, indolent and aggressive variants have been described.
T5 365-466 Sentence denotes In addition, SM patients may acquire an associated hematologic clonal non-MC lineage disease (AHNMD).
T6 467-602 Sentence denotes In some cases, hematologic parameters are indicative of slowly progressing SM although the clinical course remains indolent over years.
T7 603-655 Sentence denotes These cases have been referred to as smouldering SM.
T8 656-891 Sentence denotes We report on a smouldering patient presenting with typical skin lesions, hypercellular marrow with focal MC aggregates, persistent leukocytosis (20,000-30,000/microl) with eosinophilia (5-10%), marked lymphadenopathy, and splenomegaly.
T9 892-953 Sentence denotes The C-KIT mutation Asp-816-Val confirmed the diagnosis of SM.
T10 954-1100 Sentence denotes The clinical picture remained stable during an observation period of 10 years without signs of progression to an AHNMD or a high grade MC disease.
T11 1101-1275 Sentence denotes These data show that some patients with SM can remain in a clinically indolent smouldering state over years even when presenting with marked eosinophilia and lymphadenopathy.

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 100-112 HP_0100495 denotes mastocytosis
T2 158-173 HP_0001507 denotes abnormal growth
T3 245-261 HP_0000951 denotes skin involvement
T4 324-334 HP_0000718 denotes aggressive
T5 787-799 HP_0001974 denotes leukocytosis
T6 828-840 HP_0001880 denotes eosinophilia
T7 857-872 HP_0002716 denotes lymphadenopathy
T8 878-890 HP_0001744 denotes splenomegaly
T9 1242-1254 HP_0001880 denotes eosinophilia
T10 1259-1274 HP_0002716 denotes lymphadenopathy

PennBioIE

Id Subject Object Predicate Lexical cue
T1 896-901 protein denotes C-KIT
T2 902-910 protein denotes mutation
T3 911-914 protein denotes Asp
T4 915-918 protein denotes 816
T5 919-922 protein denotes Val

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
12007509-7#19#30#geners121913507 911-922 geners121913507 denotes Asp-816-Val
12007509-7#58#60#diseaseC0221013 950-952 diseaseC0221013 denotes SM
19#30#geners12191350758#60#diseaseC0221013 12007509-7#19#30#geners121913507 12007509-7#58#60#diseaseC0221013 associated_with Asp-816-Val,SM

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
12007509-7#4#9#gene3815 896-901 gene3815 denotes C-KIT
12007509-7#58#60#diseaseC0221013 950-952 diseaseC0221013 denotes SM
4#9#gene381558#60#diseaseC0221013 12007509-7#4#9#gene3815 12007509-7#58#60#diseaseC0221013 associated_with C-KIT,SM

performance-test

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 222-228 http://purl.obolibrary.org/obo/UBERON_0000062 denotes organs
PD-UBERON-AE-B_T2 51-56 http://purl.obolibrary.org/obo/UBERON_0000178 denotes blood

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 100-112 HP:0100495 denotes mastocytosis
TI1 22-34 HP:0100495 denotes mastocytosis
TI2 57-69 HP:0001880 denotes eosinophilia
TI3 74-89 HP:0002716 denotes lymphadenopathy
AB2 787-799 HP:0001974 denotes leukocytosis
AB3 828-840 HP:0001880 denotes eosinophilia
AB4 857-872 HP:0002716 denotes lymphadenopathy
AB5 878-890 HP:0001744 denotes splenomegaly
AB6 1242-1254 HP:0001880 denotes eosinophilia
AB7 1259-1274 HP:0002716 denotes lymphadenopathy

UBERON-AE

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 51-56 http://purl.obolibrary.org/obo/UBERON_0000178 denotes blood
PD-UBERON-AE-B_T2 222-228 http://purl.obolibrary.org/obo/UBERON_0000062 denotes organs

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 911-914 ORDO:63442 denotes Asp

DisGeNET

Id Subject Object Predicate Lexical cue
T0 896-901 gene:3815 denotes C-KIT
T1 950-952 disease:C0221013 denotes SM
R1 T0 T1 associated_with C-KIT,SM