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PubMed:3578281 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 645-655 gene:7299 denotes tyrosinase
T1 744-747 disease:C0032897 denotes PWS
T2 645-655 gene:7299 denotes tyrosinase
T3 777-793 disease:C0162835 denotes hypopigmentation
T4 645-655 gene:7299 denotes tyrosinase
T5 777-793 disease:C1876214 denotes hypopigmentation
R1 T0 T1 associated_with tyrosinase,PWS
R2 T2 T3 associated_with tyrosinase,hypopigmentation
R3 T4 T5 associated_with tyrosinase,hypopigmentation

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
3578281-5#9#19#gene7299 645-655 gene7299 denotes tyrosinase
3578281-5#108#111#diseaseC0032897 744-747 diseaseC0032897 denotes PWS
9#19#gene7299108#111#diseaseC0032897 3578281-5#9#19#gene7299 3578281-5#108#111#diseaseC0032897 associated_with tyrosinase,PWS

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 0-16 DiseaseClass:D017496 denotes Hypopigmentation
T2 24-45 SpecificDisease:D011218 denotes Prader-Willi syndrome
T3 47-80 CompositeMention:D010859 denotes Cutaneous and ocular pigmentation
T4 123-144 SpecificDisease:D011218 denotes Prader-Willi syndrome
T5 146-149 SpecificDisease:D011218 denotes PWS
T6 165-181 DiseaseClass:D017496 denotes hypopigmentation
T7 368-371 Modifier:D011218 denotes PWS
T8 389-402 Modifier:D017496 denotes hypopigmented
T9 420-436 DiseaseClass:D017496 denotes hypopigmentation
T10 618-634 DiseaseClass:D017496 denotes hypopigmentation
T11 744-747 Modifier:D011218 denotes PWS
T12 777-793 DiseaseClass:D017496 denotes hypopigmentation
T13 850-866 DiseaseClass:D017496 denotes hypopigmentation
T14 924-927 SpecificDisease:D011218 denotes PWS
T15 941-957 DiseaseClass:D017496 denotes hypopigmentation
T16 1048-1064 DiseaseClass:D017496 denotes hypopigmentation

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T4671 0-16 DiseaseClass denotes Hypopigmentation D017496
T4672 24-45 SpecificDisease denotes Prader-Willi syndrome D011218
T4673 47-80 CompositeMention denotes Cutaneous and ocular pigmentation D010859
T4674 123-144 SpecificDisease denotes Prader-Willi syndrome D011218
T4675 146-149 SpecificDisease denotes PWS D011218
T4676 165-181 DiseaseClass denotes hypopigmentation D017496
T4677 368-371 Modifier denotes PWS D011218
T4678 389-402 Modifier denotes hypopigmented D017496
T4679 420-436 DiseaseClass denotes hypopigmentation D017496
T4680 618-634 DiseaseClass denotes hypopigmentation D017496
T4681 744-747 Modifier denotes PWS D011218
T4682 777-793 DiseaseClass denotes hypopigmentation D017496
T4683 850-866 DiseaseClass denotes hypopigmentation D017496
T4684 924-927 SpecificDisease denotes PWS D011218
T4685 941-957 DiseaseClass denotes hypopigmentation D017496
T4686 1048-1064 DiseaseClass denotes hypopigmentation D017496

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T4671 0-16 DiseaseClass denotes Hypopigmentation D017496
T4672 24-45 SpecificDisease denotes Prader-Willi syndrome D011218
T4673 47-80 CompositeMention denotes Cutaneous and ocular pigmentation D010859
T4674 123-144 SpecificDisease denotes Prader-Willi syndrome D011218
T4675 146-149 SpecificDisease denotes PWS D011218
T4676 165-181 DiseaseClass denotes hypopigmentation D017496
T4677 368-371 Modifier denotes PWS D011218
T4678 389-402 Modifier denotes hypopigmented D017496
T4679 420-436 DiseaseClass denotes hypopigmentation D017496
T4680 618-634 DiseaseClass denotes hypopigmentation D017496
T4681 744-747 Modifier denotes PWS D011218
T4682 777-793 DiseaseClass denotes hypopigmentation D017496
T4683 850-866 DiseaseClass denotes hypopigmentation D017496
T4684 924-927 SpecificDisease denotes PWS D011218
T4685 941-957 DiseaseClass denotes hypopigmentation D017496
T4686 1048-1064 DiseaseClass denotes hypopigmentation D017496

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 24-45 SpecificDisease denotes Prader-Willi syndrome
T2 123-144 SpecificDisease denotes Prader-Willi syndrome
T3 146-149 SpecificDisease denotes PWS
T4 165-181 DiseaseClass denotes hypopigmentation
T5 368-371 SpecificDisease denotes PWS
T6 389-402 DiseaseClass denotes hypopigmented
T7 420-436 DiseaseClass denotes hypopigmentation
T8 618-634 DiseaseClass denotes hypopigmentation
T9 744-747 SpecificDisease denotes PWS
T10 777-793 DiseaseClass denotes hypopigmentation
T11 850-866 DiseaseClass denotes hypopigmentation
T12 924-927 SpecificDisease denotes PWS
T13 941-957 DiseaseClass denotes hypopigmentation
T14 1048-1064 DiseaseClass denotes hypopigmentation

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 24-45 SpecificDisease denotes Prader-Willi syndrome
T2 123-144 SpecificDisease denotes Prader-Willi syndrome
T3 146-149 SpecificDisease denotes PWS
T4 165-181 DiseaseClass denotes hypopigmentation
T5 368-371 SpecificDisease denotes PWS
T6 389-402 DiseaseClass denotes hypopigmented
T7 420-436 DiseaseClass denotes hypopigmentation
T8 618-634 DiseaseClass denotes hypopigmentation
T9 744-747 SpecificDisease denotes PWS
T10 777-793 DiseaseClass denotes hypopigmentation
T11 850-866 DiseaseClass denotes hypopigmentation
T12 924-927 SpecificDisease denotes PWS
T13 941-957 DiseaseClass denotes hypopigmentation
T14 1048-1064 DiseaseClass denotes hypopigmentation

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 0-16 DiseaseClass denotes Hypopigmentation
T2 24-45 SpecificDisease denotes Prader-Willi syndrome
T3 123-144 SpecificDisease denotes Prader-Willi syndrome
T4 165-181 DiseaseClass denotes hypopigmentation
T5 389-402 DiseaseClass denotes hypopigmented
T6 420-436 DiseaseClass denotes hypopigmentation
T7 618-634 DiseaseClass denotes hypopigmentation
T8 777-793 DiseaseClass denotes hypopigmentation
T9 850-866 DiseaseClass denotes hypopigmentation
T10 941-957 DiseaseClass denotes hypopigmentation
T11 1048-1064 DiseaseClass denotes hypopigmentation

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 0-45 CompositeMention denotes Hypopigmentation in the Prader-Willi syndrome
T2 68-80 CompositeMention denotes pigmentation
T3 123-150 SpecificDisease denotes Prader-Willi syndrome (PWS)
T4 165-181 CompositeMention denotes hypopigmentation
T5 389-402 CompositeMention denotes hypopigmented
T6 420-436 CompositeMention denotes hypopigmentation
T7 618-634 CompositeMention denotes hypopigmentation
T8 777-793 CompositeMention denotes hypopigmentation
T9 850-866 CompositeMention denotes hypopigmentation
T10 941-957 CompositeMention denotes hypopigmentation
T11 1048-1064 CompositeMention denotes hypopigmentation