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PubMed:1346773 JSONTXT

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DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
1346773-4#112#116#gene7076 738-742 gene7076 denotes TIMP
1346773-4#166#170#gene7076 792-796 gene7076 denotes TIMP
1346773-4#172#177#gene4943 798-803 gene4943 denotes OATL1
1346773-4#58#61#diseaseC0043194 684-687 diseaseC0043194 denotes WAS
112#116#gene707658#61#diseaseC0043194 1346773-4#112#116#gene7076 1346773-4#58#61#diseaseC0043194 associated_with TIMP,WAS
166#170#gene707658#61#diseaseC0043194 1346773-4#166#170#gene7076 1346773-4#58#61#diseaseC0043194 associated_with TIMP,WAS
172#177#gene494358#61#diseaseC0043194 1346773-4#172#177#gene4943 1346773-4#58#61#diseaseC0043194 associated_with OATL1,WAS

performance-test

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 217-220 http://purl.obolibrary.org/obo/UBERON_0001460 denotes arm

UBERON-AE

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 217-220 http://purl.obolibrary.org/obo/UBERON_0001460 denotes arm

PubCasesORDO

Id Subject Object Predicate Lexical cue
TI1 4-28 ORDO:906 denotes Wiskott-Aldrich syndrome

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-132 Sentence denotes The Wiskott-Aldrich syndrome: refinement of the localization on Xp and identification of another closely linked marker locus, OATL1.
TextSentencer_T2 133-273 Sentence denotes The Wiskott-Aldrich syndrome (WAS) has previously been mapped to the proximal short arm of the X chromosome between the DXS14 and DXS7 loci.
TextSentencer_T3 274-419 Sentence denotes In this study, further segregation analysis has been performed using a newly identified WAS family as well as an additional marker probe, HOATL1.
TextSentencer_T4 420-625 Sentence denotes The results indicate close linkage between the WAS and OATL1 loci (Z = 6.08 at theta = 0.00) and localize the TIMP, OATL1, DXS255, and WAS loci distal to DXS146 and the OATL1 and WAS loci proximal to TIMP.
TextSentencer_T5 626-825 Sentence denotes These linkage data narrow the boundaries within which the WAS locus maps to the chromosomal region bracketed by TIMP and DXS146 and support the loci order Xpter-DXS7-TIMP-(OATL1, WAS, DXS255)-DXS146.
T1 0-132 Sentence denotes The Wiskott-Aldrich syndrome: refinement of the localization on Xp and identification of another closely linked marker locus, OATL1.
T2 133-273 Sentence denotes The Wiskott-Aldrich syndrome (WAS) has previously been mapped to the proximal short arm of the X chromosome between the DXS14 and DXS7 loci.
T3 274-419 Sentence denotes In this study, further segregation analysis has been performed using a newly identified WAS family as well as an additional marker probe, HOATL1.
T4 420-625 Sentence denotes The results indicate close linkage between the WAS and OATL1 loci (Z = 6.08 at theta = 0.00) and localize the TIMP, OATL1, DXS255, and WAS loci distal to DXS146 and the OATL1 and WAS loci proximal to TIMP.
T5 626-825 Sentence denotes These linkage data narrow the boundaries within which the WAS locus maps to the chromosomal region bracketed by TIMP and DXS146 and support the loci order Xpter-DXS7-TIMP-(OATL1, WAS, DXS255)-DXS146.

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 4-28 SpecificDisease:D014923 denotes Wiskott-Aldrich syndrome
T2 137-161 SpecificDisease:D014923 denotes Wiskott-Aldrich syndrome
T3 163-166 SpecificDisease:D014923 denotes WAS
T4 362-365 Modifier:D014923 denotes WAS
T5 467-470 SpecificDisease:D014923 denotes WAS
T6 555-558 Modifier:D014923 denotes WAS
T7 599-602 Modifier:D014923 denotes WAS
T8 684-687 Modifier:D014923 denotes WAS

DisGeNET

Id Subject Object Predicate Lexical cue
T0 475-480 gene:4943 denotes OATL1
T1 467-470 disease:C0043194 denotes WAS
T2 475-480 gene:4943 denotes OATL1
T3 555-558 disease:C0043194 denotes WAS
T4 475-480 gene:4943 denotes OATL1
T5 599-602 disease:C0043194 denotes WAS
T6 530-534 gene:7076 denotes TIMP
T7 467-470 disease:C0043194 denotes WAS
T8 530-534 gene:7076 denotes TIMP
T9 599-602 disease:C0043194 denotes WAS
T10 536-541 gene:4943 denotes OATL1
T11 555-558 disease:C0043194 denotes WAS
T12 620-624 gene:7076 denotes TIMP
T13 599-602 disease:C0043194 denotes WAS
T14 589-594 gene:4943 denotes OATL1
T15 555-558 disease:C0043194 denotes WAS
T16 589-594 gene:4943 denotes OATL1
T17 599-602 disease:C0043194 denotes WAS
T18 589-594 gene:4943 denotes OATL1
T19 467-470 disease:C0043194 denotes WAS
T20 738-742 gene:7076 denotes TIMP
T21 684-687 disease:C0043194 denotes WAS
T22 792-796 gene:7076 denotes TIMP
T23 684-687 disease:C0043194 denotes WAS
T24 798-803 gene:4943 denotes OATL1
T25 684-687 disease:C0043194 denotes WAS
R1 T0 T1 associated_with OATL1,WAS
R2 T2 T3 associated_with OATL1,WAS
R3 T4 T5 associated_with OATL1,WAS
R4 T6 T7 associated_with TIMP,WAS
R5 T8 T9 associated_with TIMP,WAS
R6 T10 T11 associated_with OATL1,WAS
R7 T12 T13 associated_with TIMP,WAS
R8 T14 T15 associated_with OATL1,WAS
R9 T16 T17 associated_with OATL1,WAS
R10 T18 T19 associated_with OATL1,WAS
R11 T20 T21 associated_with TIMP,WAS
R12 T22 T23 associated_with TIMP,WAS
R13 T24 T25 associated_with OATL1,WAS

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T2380 4-28 SpecificDisease denotes Wiskott-Aldrich syndrome D014923
T2381 137-161 SpecificDisease denotes Wiskott-Aldrich syndrome D014923
T2382 163-166 SpecificDisease denotes WAS D014923
T2383 362-365 Modifier denotes WAS D014923
T2384 467-470 SpecificDisease denotes WAS D014923
T2385 555-558 Modifier denotes WAS D014923
T2386 599-602 Modifier denotes WAS D014923
T2387 684-687 Modifier denotes WAS D014923

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T2380 4-28 SpecificDisease denotes Wiskott-Aldrich syndrome D014923
T2381 137-161 SpecificDisease denotes Wiskott-Aldrich syndrome D014923
T2382 163-166 SpecificDisease denotes WAS D014923
T2383 362-365 Modifier denotes WAS D014923
T2384 467-470 SpecificDisease denotes WAS D014923
T2385 555-558 Modifier denotes WAS D014923
T2386 599-602 Modifier denotes WAS D014923
T2387 684-687 Modifier denotes WAS D014923

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 4-28 SpecificDisease denotes Wiskott-Aldrich syndrome
T2 137-161 SpecificDisease denotes Wiskott-Aldrich syndrome
T3 362-365 Modifier denotes WAS
T4 467-470 SpecificDisease denotes WAS
T5 555-558 SpecificDisease denotes WAS
T6 599-602 SpecificDisease denotes WAS
T7 684-687 SpecificDisease denotes WAS
T8 805-808 SpecificDisease denotes WAS

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 4-28 SpecificDisease denotes Wiskott-Aldrich syndrome
T2 137-161 SpecificDisease denotes Wiskott-Aldrich syndrome

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 4-28 SpecificDisease denotes Wiskott-Aldrich syndrome
T2 137-161 SpecificDisease denotes Wiskott-Aldrich syndrome

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 4-28 SpecificDisease denotes Wiskott-Aldrich syndrome
T2 137-161 SpecificDisease denotes Wiskott-Aldrich syndrome