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PubMed:16410744 JSONTXT

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PubTator4TogoVar

Id Subject Object Predicate Lexical cue proteinmutation
16410744_0 1499-1516 ProteinMutation denotes codon 787 CAG/CAA rs1050171

LitCoin-entities-OrganismTaxon-PD

Id Subject Object Predicate Lexical cue db_id
T1 1499-1504 OrganismTaxon denotes codon NCBItxid:79338

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-54 Sentence denotes Genetic alterations in primary glioblastomas in Japan.
T2 55-223 Sentence denotes Current knowledge of genetic alterations in glioblastomas is based largely on genetic analyses of tumors from mainly caucasian patients in the United States and Europe.
T3 224-365 Sentence denotes In the present study, screening for several key genetic alterations was performed on 77 primary (de novo) glioblastomas in Japanese patients.
T4 366-506 Sentence denotes SSCP followed by DNA sequencing revealed TP53 mutations in 16 of 73 (22%) glioblastomas and PTEN mutations in 13 of 63 (21%) cases analyzed.
T5 507-641 Sentence denotes Polymerase chain reaction (PCR) showed EGFR amplification in 25 of 77 (32%) cases and p16 homozygous deletion in 32 of 77 (42%) cases.
T6 642-728 Sentence denotes Quantitative microsatellite analysis revealed LOH 10q in 41 of 59 (69%) glioblastomas.
T7 729-870 Sentence denotes The frequencies of these genetic alterations were similar to those reported for primary glioblastomas at the population level in Switzerland.
T8 871-1128 Sentence denotes As previously observed for glioblastomas in Europe, there was a positive association between EGFR amplification and p16 deletion (p=0.009), whereas there was an inverse association between TP53 mutations and p16 deletion (p=0.049) in glioblastomas in Japan.
T9 1129-1260 Sentence denotes Multivariate analyses showed that radiotherapy was significantly predictive for longer survival of glioblastoma patients (p=0.002).
T10 1261-1455 Sentence denotes SSCP followed by DNA sequencing of the kinase domain (exons 18-21) of the EGFR gene revealed mutations in 2 ou of 69 (3%) glioblastomas in Japan and in 4 of 81 (5%) glioblastomas in Switzerland.
T11 1456-1797 Sentence denotes The allele frequencies of polymorphisms at codon 787 CAG/CAA (Gln/Gln) in glioblastomas in Japan were G/G (82.4%), G/A (10.8%), A/A (6.8%), corresponding to G 0.878 versus A 0.122, significantly different from those in glioblastomas in Switzerland: G/G (27.2%), G/A (28.4%), A/A (44.4%), corresponding to G 0.414 versus A 0.586 (p < 0.0001).
T12 1798-2078 Sentence denotes These results suggest that primary glioblastomas in Japan show genetic alterations similar to those in Switzerland, suggesting a similar molecular basis in caucasians and Asians, despite different genetic backgrounds, including different status of a polymorphism in the EGFR gene.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
2705 31-44 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2706 99-112 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2707 153-159 DiseaseOrPhenotypicFeature denotes tumors MESH:D009369
2708 182-190 OrganismTaxon denotes patients NCBITaxon:9606
2709 330-343 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2710 356-364 OrganismTaxon denotes patients NCBITaxon:9606
2711 407-411 GeneOrGeneProduct denotes TP53 NCBIGene:7157
2712 440-453 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2713 458-462 GeneOrGeneProduct denotes PTEN NCBIGene:5728
2714 546-550 GeneOrGeneProduct denotes EGFR NCBIGene:1956
2715 593-596 GeneOrGeneProduct denotes p16 NCBIGene:1029
2716 714-727 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2717 817-830 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2718 898-911 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2719 964-968 GeneOrGeneProduct denotes EGFR NCBIGene:1956
2720 987-990 GeneOrGeneProduct denotes p16 NCBIGene:1029
2721 1060-1064 GeneOrGeneProduct denotes TP53 NCBIGene:7157
2722 1079-1082 GeneOrGeneProduct denotes p16 NCBIGene:1029
2723 1105-1118 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2724 1228-1240 DiseaseOrPhenotypicFeature denotes glioblastoma MESH:D005909
2725 1241-1249 OrganismTaxon denotes patients NCBITaxon:9606
2726 1335-1339 GeneOrGeneProduct denotes EGFR NCBIGene:1956
2727 1383-1396 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2728 1426-1439 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2729 1499-1516 SequenceVariant denotes codon 787 CAG/CAA p|SUB|Q|787|Q
2730 1518-1525 SequenceVariant denotes Gln/Gln p|SUB|Q||Q
2731 1530-1543 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2732 1675-1688 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2733 1833-1846 DiseaseOrPhenotypicFeature denotes glioblastomas MESH:D005909
2734 2068-2072 GeneOrGeneProduct denotes EGFR NCBIGene:1956

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 31-44 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177
T2 99-112 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177
T3 330-343 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177
T4 440-453 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177
T5 714-727 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177
T6 817-830 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177
T7 898-911 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177
T8 1105-1118 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177
T9 1228-1240 DiseaseOrPhenotypicFeature denotes glioblastoma 0018177
T10 1383-1396 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177
T11 1426-1439 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177
T12 1530-1543 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177
T13 1675-1688 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177
T14 1833-1846 DiseaseOrPhenotypicFeature denotes glioblastomas 0018177

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 407-411 GeneOrGeneProduct denotes TP53
T2 458-462 GeneOrGeneProduct denotes PTEN
T3 507-517 GeneOrGeneProduct denotes Polymerase
T4 518-523 GeneOrGeneProduct denotes chain
T5 546-550 GeneOrGeneProduct denotes EGFR
T6 779-786 GeneOrGeneProduct denotes similar
T7 964-968 GeneOrGeneProduct denotes EGFR
T8 1060-1064 GeneOrGeneProduct denotes TP53
T9 1300-1306 GeneOrGeneProduct denotes kinase
T10 1335-1339 GeneOrGeneProduct denotes EGFR
T11 1518-1521 GeneOrGeneProduct denotes Gln
T12 1522-1525 GeneOrGeneProduct denotes Gln
T13 1881-1888 GeneOrGeneProduct denotes similar
T14 1927-1934 GeneOrGeneProduct denotes similar
T15 2068-2072 GeneOrGeneProduct denotes EGFR

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 116-121 GeneOrGeneProduct denotes based
T2 122-129 GeneOrGeneProduct denotes largely
T3 153-159 GeneOrGeneProduct denotes tumors
T4 165-171 GeneOrGeneProduct denotes mainly
T5 407-411 GeneOrGeneProduct denotes TP53
T6 412-421 GeneOrGeneProduct denotes mutations
T7 422-427 GeneOrGeneProduct denotes in 16
T8 458-462 GeneOrGeneProduct denotes PTEN
T9 463-472 GeneOrGeneProduct denotes mutations
T10 473-478 GeneOrGeneProduct denotes in 13
T11 491-496 GeneOrGeneProduct denotes cases
T12 507-517 GeneOrGeneProduct denotes Polymerase
T13 518-523 GeneOrGeneProduct denotes chain
T14 546-550 GeneOrGeneProduct denotes EGFR
T15 565-570 GeneOrGeneProduct denotes in 25
T16 583-588 GeneOrGeneProduct denotes cases
T17 617-622 GeneOrGeneProduct denotes in 32
T18 635-640 GeneOrGeneProduct denotes cases
T19 733-744 GeneOrGeneProduct denotes frequencies
T20 779-786 GeneOrGeneProduct denotes similar
T21 964-968 GeneOrGeneProduct denotes EGFR
T22 1060-1064 GeneOrGeneProduct denotes TP53
T23 1065-1074 GeneOrGeneProduct denotes mutations
T24 1194-1204 GeneOrGeneProduct denotes predictive
T25 1300-1306 GeneOrGeneProduct denotes kinase
T26 1335-1339 GeneOrGeneProduct denotes EGFR
T27 1354-1368 GeneOrGeneProduct denotes mutations in 2
T28 1406-1414 GeneOrGeneProduct denotes and in 4
T29 1467-1478 GeneOrGeneProduct denotes frequencies
T30 1509-1512 GeneOrGeneProduct denotes CAG
T31 1518-1521 GeneOrGeneProduct denotes Gln
T32 1522-1525 GeneOrGeneProduct denotes Gln
T33 1881-1888 GeneOrGeneProduct denotes similar
T34 1927-1934 GeneOrGeneProduct denotes similar
T35 1945-1950 GeneOrGeneProduct denotes basis
T36 2068-2072 GeneOrGeneProduct denotes EGFR

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 31-44 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T2 99-112 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T3 153-159 DiseaseOrPhenotypicFeature denotes tumors D009369
T4 330-343 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T5 440-453 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T6 714-727 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T7 817-830 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T8 898-911 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T9 1105-1118 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T10 1228-1240 DiseaseOrPhenotypicFeature denotes glioblastoma D005909
T11 1383-1396 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T12 1426-1439 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T13 1530-1543 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T14 1675-1688 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T15 1833-1846 DiseaseOrPhenotypicFeature denotes glioblastomas D005909

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 407-411 GeneOrGeneProduct denotes TP53
T2 458-462 GeneOrGeneProduct denotes PTEN
T3 546-550 GeneOrGeneProduct denotes EGFR
T4 964-968 GeneOrGeneProduct denotes EGFR
T5 1060-1064 GeneOrGeneProduct denotes TP53
T6 1335-1339 GeneOrGeneProduct denotes EGFR
T7 1518-1521 GeneOrGeneProduct denotes Gln
T8 1522-1525 GeneOrGeneProduct denotes Gln
T9 2068-2072 GeneOrGeneProduct denotes EGFR

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 1228-1240 DiseaseOrPhenotypicFeature denotes glioblastoma 0020690|0018177
T3 1513-1516 DiseaseOrPhenotypicFeature denotes CAA 0011921

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 31-44 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T2 99-112 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T3 153-159 DiseaseOrPhenotypicFeature denotes tumors DISEASE|D009369
T5 330-343 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T6 440-453 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T7 714-727 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T8 817-830 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T9 898-911 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T10 1105-1118 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T11 1228-1240 DiseaseOrPhenotypicFeature denotes glioblastoma D005909
T12 1383-1396 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T13 1426-1439 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T14 1530-1543 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T15 1675-1688 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T16 1833-1846 DiseaseOrPhenotypicFeature denotes glioblastomas D005909

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 31-44 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T2 99-112 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T3 153-159 DiseaseOrPhenotypicFeature denotes tumors D009369
T4 330-343 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T5 440-453 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T6 714-727 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T7 817-830 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T8 898-911 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T9 1105-1118 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T10 1228-1240 DiseaseOrPhenotypicFeature denotes glioblastoma D005909
T11 1383-1396 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T12 1426-1439 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T13 1530-1543 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T14 1675-1688 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T15 1833-1846 DiseaseOrPhenotypicFeature denotes glioblastomas D005909

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 1513-1516 ChemicalEntity denotes CAA http://purl.obolibrary.org/obo/CHEBI_27869
T2 1518-1521 ChemicalEntity denotes Gln http://purl.obolibrary.org/obo/CHEBI_30011
T3 1522-1525 ChemicalEntity denotes Gln http://purl.obolibrary.org/obo/CHEBI_30011

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 182-190 OrganismTaxon denotes patients
T2 356-364 OrganismTaxon denotes patients
T3 1241-1249 OrganismTaxon denotes patients

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T3 1522-1525 ChemicalEntity denotes Gln http://purl.obolibrary.org/obo/CHEBI_30011
T2 1518-1521 ChemicalEntity denotes Gln http://purl.obolibrary.org/obo/CHEBI_30011
T1 1513-1516 ChemicalEntity denotes CAA http://purl.obolibrary.org/obo/CHEBI_27869
T9 2068-2072 GeneOrGeneProduct denotes EGFR
T8 1522-1525 GeneOrGeneProduct denotes Gln
T7 1518-1521 GeneOrGeneProduct denotes Gln
T6 1335-1339 GeneOrGeneProduct denotes EGFR
T5 1060-1064 GeneOrGeneProduct denotes TP53
T4 964-968 GeneOrGeneProduct denotes EGFR
T10010 546-550 GeneOrGeneProduct denotes EGFR
T43778 458-462 GeneOrGeneProduct denotes PTEN
T84461 407-411 GeneOrGeneProduct denotes TP53
T15 1833-1846 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T14 1675-1688 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T13 1530-1543 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T12 1426-1439 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T11 1383-1396 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T10 1228-1240 DiseaseOrPhenotypicFeature denotes glioblastoma D005909
T82858 1105-1118 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T38489 898-911 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T92957 817-830 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T82940 714-727 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T36892 440-453 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T93017 330-343 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T70777 153-159 DiseaseOrPhenotypicFeature denotes tumors D009369
T55819 99-112 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T87053 31-44 DiseaseOrPhenotypicFeature denotes glioblastomas D005909
T62246 1241-1249 OrganismTaxon denotes patients
T78491 356-364 OrganismTaxon denotes patients
T42372 182-190 OrganismTaxon denotes patients

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 99-112 HP_0100843 denotes glioblastomas
T2 153-159 HP_0002664 denotes tumors
T3 330-343 HP_0100843 denotes glioblastomas
T4 440-453 HP_0100843 denotes glioblastomas
T5 714-727 HP_0100843 denotes glioblastomas
T6 817-830 HP_0100843 denotes glioblastomas
T7 898-911 HP_0100843 denotes glioblastomas
T8 1105-1118 HP_0100843 denotes glioblastomas
T9 1228-1240 HP_0100843 denotes glioblastoma
T10 1383-1396 HP_0100843 denotes glioblastomas
T11 1426-1439 HP_0100843 denotes glioblastomas
T12 1530-1543 HP_0100843 denotes glioblastomas
T13 1675-1688 HP_0100843 denotes glioblastomas
T14 1833-1846 HP_0100843 denotes glioblastomas

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
16410744-10#57#60#gene10194 1513-1516 gene10194 denotes CAA
16410744-10#219#232#diseaseC0017636 1675-1688 diseaseC0017636 denotes glioblastomas
16410744-11#270#274#gene1956 2068-2072 gene1956 denotes EGFR
16410744-11#35#48#diseaseC0017636 1833-1846 diseaseC0017636 denotes glioblastomas
16410744-3#92#96#gene5728 458-462 gene5728 denotes PTEN
16410744-3#74#87#diseaseC0017636 440-453 diseaseC0017636 denotes glioblastomas
16410744-7#116#119#gene1029 987-990 gene1029 denotes p16
16410744-7#189#193#gene7157 1060-1064 gene7157 denotes TP53
16410744-7#208#211#gene1029 1079-1082 gene1029 denotes p16
16410744-7#27#40#diseaseC0017636 898-911 diseaseC0017636 denotes glioblastomas
16410744-7#234#247#diseaseC0017636 1105-1118 diseaseC0017636 denotes glioblastomas
16410744-7#27#40#diseaseC0017636 898-911 diseaseC0017636 denotes glioblastomas
16410744-7#234#247#diseaseC0017636 1105-1118 diseaseC0017636 denotes glioblastomas
16410744-7#27#40#diseaseC0017636 898-911 diseaseC0017636 denotes glioblastomas
16410744-7#234#247#diseaseC0017636 1105-1118 diseaseC0017636 denotes glioblastomas
57#60#gene10194219#232#diseaseC0017636 16410744-10#57#60#gene10194 16410744-10#219#232#diseaseC0017636 associated_with CAA,glioblastomas
270#274#gene195635#48#diseaseC0017636 16410744-11#270#274#gene1956 16410744-11#35#48#diseaseC0017636 associated_with EGFR,glioblastomas
92#96#gene572874#87#diseaseC0017636 16410744-3#92#96#gene5728 16410744-3#74#87#diseaseC0017636 associated_with PTEN,glioblastomas
116#119#gene102927#40#diseaseC0017636 16410744-7#116#119#gene1029 16410744-7#27#40#diseaseC0017636 associated_with p16,glioblastomas
116#119#gene1029234#247#diseaseC0017636 16410744-7#116#119#gene1029 16410744-7#234#247#diseaseC0017636 associated_with p16,glioblastomas
116#119#gene102927#40#diseaseC0017636 16410744-7#116#119#gene1029 16410744-7#27#40#diseaseC0017636 associated_with p16,glioblastomas
116#119#gene1029234#247#diseaseC0017636 16410744-7#116#119#gene1029 16410744-7#234#247#diseaseC0017636 associated_with p16,glioblastomas
116#119#gene102927#40#diseaseC0017636 16410744-7#116#119#gene1029 16410744-7#27#40#diseaseC0017636 associated_with p16,glioblastomas
116#119#gene1029234#247#diseaseC0017636 16410744-7#116#119#gene1029 16410744-7#234#247#diseaseC0017636 associated_with p16,glioblastomas
189#193#gene715727#40#diseaseC0017636 16410744-7#189#193#gene7157 16410744-7#27#40#diseaseC0017636 associated_with TP53,glioblastomas
189#193#gene7157234#247#diseaseC0017636 16410744-7#189#193#gene7157 16410744-7#234#247#diseaseC0017636 associated_with TP53,glioblastomas
189#193#gene715727#40#diseaseC0017636 16410744-7#189#193#gene7157 16410744-7#27#40#diseaseC0017636 associated_with TP53,glioblastomas
189#193#gene7157234#247#diseaseC0017636 16410744-7#189#193#gene7157 16410744-7#234#247#diseaseC0017636 associated_with TP53,glioblastomas
189#193#gene715727#40#diseaseC0017636 16410744-7#189#193#gene7157 16410744-7#27#40#diseaseC0017636 associated_with TP53,glioblastomas
189#193#gene7157234#247#diseaseC0017636 16410744-7#189#193#gene7157 16410744-7#234#247#diseaseC0017636 associated_with TP53,glioblastomas
208#211#gene102927#40#diseaseC0017636 16410744-7#208#211#gene1029 16410744-7#27#40#diseaseC0017636 associated_with p16,glioblastomas
208#211#gene1029234#247#diseaseC0017636 16410744-7#208#211#gene1029 16410744-7#234#247#diseaseC0017636 associated_with p16,glioblastomas
208#211#gene102927#40#diseaseC0017636 16410744-7#208#211#gene1029 16410744-7#27#40#diseaseC0017636 associated_with p16,glioblastomas
208#211#gene1029234#247#diseaseC0017636 16410744-7#208#211#gene1029 16410744-7#234#247#diseaseC0017636 associated_with p16,glioblastomas
208#211#gene102927#40#diseaseC0017636 16410744-7#208#211#gene1029 16410744-7#27#40#diseaseC0017636 associated_with p16,glioblastomas
208#211#gene1029234#247#diseaseC0017636 16410744-7#208#211#gene1029 16410744-7#234#247#diseaseC0017636 associated_with p16,glioblastomas

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 1499-1516 DNAMutation:|SUB|CAG|CODON787|CAA denotes codon 787 CAG/CAA

DisGeNET

Id Subject Object Predicate Lexical cue
T0 407-411 gene:7157 denotes TP53
T1 440-453 disease:C0017636 denotes glioblastomas
T2 458-462 gene:5728 denotes PTEN
T3 440-453 disease:C0017636 denotes glioblastomas
T4 1335-1339 gene:1956 denotes EGFR
T5 1383-1396 disease:C0017636 denotes glioblastomas
T6 1335-1339 gene:1956 denotes EGFR
T7 1426-1439 disease:C0017636 denotes glioblastomas
R1 T0 T1 associated_with TP53,glioblastomas
R2 T2 T3 associated_with PTEN,glioblastomas
R3 T4 T5 associated_with EGFR,glioblastomas
R4 T6 T7 associated_with EGFR,glioblastomas