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PubMed:11574907 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 91-114 DiseaseOrPhenotypicFeature denotes oculocutaneous albinism 0018910
T2 116-120 DiseaseOrPhenotypicFeature denotes OCA4 0011683
T3 122-145 DiseaseOrPhenotypicFeature denotes Oculocutaneous albinism 0018910
T4 147-150 DiseaseOrPhenotypicFeature denotes OCA 0018910
T5 214-217 DiseaseOrPhenotypicFeature denotes OCA 0018910
T6 238-254 DiseaseOrPhenotypicFeature denotes hypopigmentation 0007459
T7 343-352 DiseaseOrPhenotypicFeature denotes nystagmus 0005712
T8 366-376 DiseaseOrPhenotypicFeature denotes strabismus 0003432
T9 433-437 DiseaseOrPhenotypicFeature denotes skin 0002531
T10 469-480 DiseaseOrPhenotypicFeature denotes skin cancer 0002898
T11 526-529 DiseaseOrPhenotypicFeature denotes OCA 0018910
T12 551-555 DiseaseOrPhenotypicFeature denotes OCA1 0018135
T13 736-739 DiseaseOrPhenotypicFeature denotes OCA 0018910
T14 751-755 DiseaseOrPhenotypicFeature denotes OCA2 0008746
T15 794-797 DiseaseOrPhenotypicFeature denotes OCA 0018910
T16 880-883 DiseaseOrPhenotypicFeature denotes OCA 0018910
T17 895-899 DiseaseOrPhenotypicFeature denotes OCA3 0008747
T18 929-932 DiseaseOrPhenotypicFeature denotes OCA 0018910
T19 963-971 DiseaseOrPhenotypicFeature denotes albinism 0043209
T20 1102-1105 DiseaseOrPhenotypicFeature denotes OCA 0018910
T21 1155-1158 DiseaseOrPhenotypicFeature denotes OCA 0018910
T22 1272-1275 DiseaseOrPhenotypicFeature denotes OCA 0018910
T23 1285-1289 DiseaseOrPhenotypicFeature denotes OCA4 0011683

FSU-PRGE

Id Subject Object Predicate Lexical cue
T1 47-57 protein denotes underwhite
T2 64-66 protein denotes uw
T3 605-608 protein denotes TYR
T4 623-633 protein denotes tyrosinase
T5 835-836 protein denotes P
T6 1006-1011 protein denotes TYRP1
T7 1022-1050 protein denotes tyrosinase-related protein 1
T8 1069-1072 protein denotes TYR
T9 1077-1078 protein denotes P
T10 1189-1199 protein denotes underwhite
T11 1206-1208 protein denotes uw
T12 1313-1317 protein denotes MATP
T13 1324-1363 protein denotes membrane-associated transporter protein

PIR-corpus2

Id Subject Object Predicate Lexical cue
T1 605-608 protein denotes TYR
T2 623-633 protein denotes tyrosinase
T3 1006-1011 protein denotes TYRP1
T4 1022-1050 protein denotes tyrosinase-related protein 1
T5 1069-1072 protein denotes TYR
T6 1313-1317 protein denotes MATP
T7 1324-1355 protein denotes membrane-associated transporter
T8 1435-1446 protein denotes transporter

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
11574907-0#47#57#gene51151 47-57 gene51151 denotes underwhite
11574907-0#91#114#diseaseC0078918 91-114 diseaseC0078918 denotes oculocutaneous albinism
11574907-7#0#4#gene4948 751-755 gene4948 denotes OCA2
11574907-7#43#46#diseaseC0078918 794-797 diseaseC0078918 denotes OCA
11574907-7#129#132#diseaseC0078918 880-883 diseaseC0078918 denotes OCA
11574907-8#0#4#gene7306 895-899 gene7306 denotes OCA3
11574907-8#111#116#gene7306 1004-1009 gene7306 denotes n TYR
11574907-8#127#155#gene7306 1020-1048 gene7306 denotes g tyrosinase-related protein
11574907-8#34#37#diseaseC0078918 929-932 diseaseC0078918 denotes OCA
11574907-8#68#76#diseaseC0001916 962-970 diseaseC0001916 denotes albinis
11574907-8#34#37#diseaseC0078918 929-932 diseaseC0078918 denotes OCA
11574907-8#68#76#diseaseC0001916 962-970 diseaseC0001916 denotes albinis
11574907-8#34#37#diseaseC0078918 929-932 diseaseC0078918 denotes OCA
11574907-8#68#76#diseaseC0001916 962-970 diseaseC0001916 denotes albinis
11574907-9#16#19#gene7299 1069-1072 gene7299 denotes TYR
11574907-9#49#52#diseaseC0078918 1102-1105 diseaseC0078918 denotes OCA
11574907-9#102#105#diseaseC0078918 1155-1158 diseaseC0078918 denotes OCA
47#57#gene5115191#114#diseaseC0078918 11574907-0#47#57#gene51151 11574907-0#91#114#diseaseC0078918 associated_with underwhite,oculocutaneous albinism
0#4#gene494843#46#diseaseC0078918 11574907-7#0#4#gene4948 11574907-7#43#46#diseaseC0078918 associated_with OCA2,OCA
0#4#gene4948129#132#diseaseC0078918 11574907-7#0#4#gene4948 11574907-7#129#132#diseaseC0078918 associated_with OCA2,OCA
0#4#gene730634#37#diseaseC0078918 11574907-8#0#4#gene7306 11574907-8#34#37#diseaseC0078918 associated_with OCA3,OCA
0#4#gene730668#76#diseaseC0001916 11574907-8#0#4#gene7306 11574907-8#68#76#diseaseC0001916 associated_with OCA3, albinis
0#4#gene730634#37#diseaseC0078918 11574907-8#0#4#gene7306 11574907-8#34#37#diseaseC0078918 associated_with OCA3,OCA
0#4#gene730668#76#diseaseC0001916 11574907-8#0#4#gene7306 11574907-8#68#76#diseaseC0001916 associated_with OCA3, albinis
0#4#gene730634#37#diseaseC0078918 11574907-8#0#4#gene7306 11574907-8#34#37#diseaseC0078918 associated_with OCA3,OCA
0#4#gene730668#76#diseaseC0001916 11574907-8#0#4#gene7306 11574907-8#68#76#diseaseC0001916 associated_with OCA3, albinis
111#116#gene730634#37#diseaseC0078918 11574907-8#111#116#gene7306 11574907-8#34#37#diseaseC0078918 associated_with n TYR,OCA
111#116#gene730668#76#diseaseC0001916 11574907-8#111#116#gene7306 11574907-8#68#76#diseaseC0001916 associated_with n TYR, albinis
111#116#gene730634#37#diseaseC0078918 11574907-8#111#116#gene7306 11574907-8#34#37#diseaseC0078918 associated_with n TYR,OCA
111#116#gene730668#76#diseaseC0001916 11574907-8#111#116#gene7306 11574907-8#68#76#diseaseC0001916 associated_with n TYR, albinis
111#116#gene730634#37#diseaseC0078918 11574907-8#111#116#gene7306 11574907-8#34#37#diseaseC0078918 associated_with n TYR,OCA
111#116#gene730668#76#diseaseC0001916 11574907-8#111#116#gene7306 11574907-8#68#76#diseaseC0001916 associated_with n TYR, albinis
127#155#gene730634#37#diseaseC0078918 11574907-8#127#155#gene7306 11574907-8#34#37#diseaseC0078918 associated_with g tyrosinase-related protein,OCA
127#155#gene730668#76#diseaseC0001916 11574907-8#127#155#gene7306 11574907-8#68#76#diseaseC0001916 associated_with g tyrosinase-related protein, albinis
127#155#gene730634#37#diseaseC0078918 11574907-8#127#155#gene7306 11574907-8#34#37#diseaseC0078918 associated_with g tyrosinase-related protein,OCA
127#155#gene730668#76#diseaseC0001916 11574907-8#127#155#gene7306 11574907-8#68#76#diseaseC0001916 associated_with g tyrosinase-related protein, albinis
127#155#gene730634#37#diseaseC0078918 11574907-8#127#155#gene7306 11574907-8#34#37#diseaseC0078918 associated_with g tyrosinase-related protein,OCA
127#155#gene730668#76#diseaseC0001916 11574907-8#127#155#gene7306 11574907-8#68#76#diseaseC0001916 associated_with g tyrosinase-related protein, albinis
16#19#gene729949#52#diseaseC0078918 11574907-9#16#19#gene7299 11574907-9#49#52#diseaseC0078918 associated_with TYR,OCA
16#19#gene7299102#105#diseaseC0078918 11574907-9#16#19#gene7299 11574907-9#102#105#diseaseC0078918 associated_with TYR,OCA

PIR-corpus1

Id Subject Object Predicate Lexical cue
T1 623-633 protein denotes tyrosinase
T2 1006-1011 acronym denotes TYRP1
T3 1022-1050 protein denotes tyrosinase-related protein 1
T4 1304-1311 protein denotes protein
T5 1313-1317 acronym denotes MATP
T6 1324-1355 protein denotes membrane-associated transporter
T7 1435-1446 protein denotes transporter

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1189-1199 gene:51151 denotes underwhite
T1 1272-1275 disease:C0078918 denotes OCA
R1 T0 T1 associated_with underwhite,OCA