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PubMed:15200408 JSONTXT

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PubTator4TogoVar

Id Subject Object Predicate Lexical cue proteinmutation
15200408_0 1495-1502 ProteinMutation denotes Ala7Val rs373513519
15200408_1 1566-1575 ProteinMutation denotes Pro154Ala rs1057353

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
890 29-34 OrganismTaxon denotes human NCBITaxon:9606
891 35-44 GeneOrGeneProduct denotes uroplakin NCBIGene:11045|NCBIGene:7380
892 54-75 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux MESH:C564042
893 137-158 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux MESH:C564042
894 160-163 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
895 170-189 DiseaseOrPhenotypicFeature denotes hereditary disorder MESH:D030342
896 343-362 DiseaseOrPhenotypicFeature denotes hereditary diseases MESH:D030342
897 379-390 DiseaseOrPhenotypicFeature denotes nephropathy MESH:D007674
898 416-439 DiseaseOrPhenotypicFeature denotes end-stage renal failure MESH:D007676
899 513-518 OrganismTaxon denotes mouse NCBITaxon:10090
900 519-537 GeneOrGeneProduct denotes uroplakin (UP) III NCBIGene:22270
901 647-650 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
902 655-669 DiseaseOrPhenotypicFeature denotes hydronephrosis MESH:D006869
903 723-725 GeneOrGeneProduct denotes UP NCBIGene:11045|NCBIGene:7380
904 753-758 OrganismTaxon denotes human NCBITaxon:9606
905 759-762 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
906 786-788 GeneOrGeneProduct denotes UP NCBIGene:11045|NCBIGene:7380
907 801-809 OrganismTaxon denotes patients NCBITaxon:9606
908 845-848 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
909 1162-1165 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
910 1214-1217 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
911 1298-1301 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
912 1302-1310 OrganismTaxon denotes patients NCBITaxon:9606
913 1425-1428 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
914 1447-1452 GeneOrGeneProduct denotes UP Ia NCBIGene:11045
915 1470-1476 SequenceVariant denotes C to T DBSNP:rs373513519
916 1495-1502 SequenceVariant denotes Ala7Val DBSNP:rs373513519
917 1523-1529 GeneOrGeneProduct denotes UP III NCBIGene:7380
918 1542-1548 SequenceVariant denotes C to G c|SUB|C||G
919 1566-1575 SequenceVariant denotes Pro154Ala p|SUB|P|154|A
920 1616-1619 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
921 1766-1772 GeneOrGeneProduct denotes UP III NCBIGene:7380
922 1781-1784 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
923 1982-1991 GeneOrGeneProduct denotes uroplakin NCBIGene:11045|NCBIGene:7380
924 2037-2040 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
925 2044-2050 OrganismTaxon denotes humans NCBITaxon:9606
926 2219-2222 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
927 2223-2231 OrganismTaxon denotes patients NCBITaxon:9606
928 2293-2299 GeneOrGeneProduct denotes UP III NCBIGene:22270
929 2309-2313 OrganismTaxon denotes mice NCBITaxon:10090
930 2347-2350 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
931 2368-2382 DiseaseOrPhenotypicFeature denotes hydronephrosis MESH:D006869
932 2387-2401 DiseaseOrPhenotypicFeature denotes neonatal death MESH:D066087
933 2437-2446 GeneOrGeneProduct denotes uroplakin NCBIGene:11045|NCBIGene:7380
934 2505-2511 OrganismTaxon denotes humans NCBITaxon:9606

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-116 Sentence denotes Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity.
T2 117-128 Sentence denotes BACKGROUND:
T3 129-265 Sentence denotes Primary vesicoureteral reflux (VUR) is a hereditary disorder characterized by the retrograde flow of urine into the ureters and kidneys.
T4 266-363 Sentence denotes It affects about 1% of the young children and is thus one of the most common hereditary diseases.
T5 364-463 Sentence denotes Its associated nephropathy is an important cause of end-stage renal failure in children and adults.
T6 464-670 Sentence denotes Recent studies indicate that genetic ablation of mouse uroplakin (UP) III gene, which encodes a 47 kD urothelial-specific integral membrane protein forming urothelial plaques, causes VUR and hydronephrosis.
T7 671-679 Sentence denotes METHODS:
T8 680-981 Sentence denotes To begin to determine whether mutations in UP genes might play a role in human VUR, we genotyped all four UP genes in 76 patients with radiologically proven primary VUR by polymerase chain reaction (PCR) amplification and sequencing of all their exons plus 50 to 150 bp of flanking intronic sequences.
T9 982-990 Sentence denotes RESULTS:
T10 991-1130 Sentence denotes Eighteen single nucleotide polymorphisms (SNPs) were identified, seven of which were missense, with no truncation or frame shift mutations.
T11 1131-1356 Sentence denotes Since healthy relatives of the VUR probands are not reliable negative controls for VUR, we used a population of 90 race-matched, healthy individuals, unrelated to the VUR patients, as controls to perform an association study.
T12 1357-1429 Sentence denotes Most of the SNPs were not found to be significantly associated with VUR.
T13 1430-1635 Sentence denotes However, SNP1 of UP Ia gene affecting a C to T conversion and an Ala7Val change, and SNP7 of UP III affecting a C to G conversion and a Pro154Ala change, were marginally associated with VUR (both P= 0.08).
T14 1636-1844 Sentence denotes Studies of additional cases yielded a second set of data that, in combination with the first set, confirmed a weak association of UP III SNP7 in VUR (P= 0.036 adjusted for both subsets of cases vs. controls).
T15 1845-1856 Sentence denotes CONCLUSION:
T16 1857-2135 Sentence denotes Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease.
T17 2136-2512 Sentence denotes The fact that no truncation or frame shift mutations have been found in any of the VUR patients, coupled with our recent finding that some breeding pairs of UP III knockout mice yield litters that show not only VUR, but also severe hydronephrosis and neonatal death, raises the possibility that major uroplakin mutations could be embryonically or postnatally lethal in humans.

LitCoin-entities-OrganismTaxon-PD

Id Subject Object Predicate Lexical cue db_id
T1 29-34 OrganismTaxon denotes human NCBItxid:9606
T2 513-518 OrganismTaxon denotes mouse NCBItxid:10090|NCBItxid:10088
T4 753-758 OrganismTaxon denotes human NCBItxid:9606
T5 2044-2050 OrganismTaxon denotes humans NCBItxid:9605
T6 2309-2313 OrganismTaxon denotes mice NCBItxid:10095|NCBItxid:10088
T8 2505-2511 OrganismTaxon denotes humans NCBItxid:9605

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 54-75 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux 0006007
T2 137-158 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux 0006007
T3 416-439 DiseaseOrPhenotypicFeature denotes end-stage renal failure 0004375
T4 655-669 DiseaseOrPhenotypicFeature denotes hydronephrosis 0005510
T5 1937-1948 DiseaseOrPhenotypicFeature denotes inheritance 0021152
T6 2368-2382 DiseaseOrPhenotypicFeature denotes hydronephrosis 0005510

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T1 1495-1502 SequenceVariant denotes Ala7Val
T2 1566-1575 SequenceVariant denotes Pro154Ala

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 0-4 GeneOrGeneProduct denotes Lack
T2 8-13 GeneOrGeneProduct denotes major
T3 54-75 GeneOrGeneProduct denotes vesicoureteral reflux
T4 137-158 GeneOrGeneProduct denotes vesicoureteral reflux
T5 160-163 GeneOrGeneProduct denotes VUR
T6 257-264 GeneOrGeneProduct denotes kidneys
T7 293-298 GeneOrGeneProduct denotes young
T8 416-419 GeneOrGeneProduct denotes end
T9 529-537 GeneOrGeneProduct denotes (UP) III
T10 586-611 GeneOrGeneProduct denotes integral membrane protein
T11 647-650 GeneOrGeneProduct denotes VUR
T12 671-678 GeneOrGeneProduct denotes METHODS
T13 683-688 GeneOrGeneProduct denotes begin
T14 692-701 GeneOrGeneProduct denotes determine
T15 710-719 GeneOrGeneProduct denotes mutations
T16 759-762 GeneOrGeneProduct denotes VUR
T17 777-780 GeneOrGeneProduct denotes all
T18 845-848 GeneOrGeneProduct denotes VUR
T19 852-862 GeneOrGeneProduct denotes polymerase
T20 863-868 GeneOrGeneProduct denotes chain
T21 916-919 GeneOrGeneProduct denotes all
T22 1076-1084 GeneOrGeneProduct denotes missense
T23 1094-1104 GeneOrGeneProduct denotes truncation
T24 1114-1119 GeneOrGeneProduct denotes shift
T25 1120-1129 GeneOrGeneProduct denotes mutations
T26 1162-1165 GeneOrGeneProduct denotes VUR
T27 1214-1217 GeneOrGeneProduct denotes VUR
T28 1246-1250 GeneOrGeneProduct denotes race
T29 1298-1301 GeneOrGeneProduct denotes VUR
T30 1425-1428 GeneOrGeneProduct denotes VUR
T31 1439-1443 GeneOrGeneProduct denotes SNP1
T32 1447-1452 GeneOrGeneProduct denotes UP Ia
T33 1523-1529 GeneOrGeneProduct denotes UP III
T34 1589-1599 GeneOrGeneProduct denotes marginally
T35 1616-1619 GeneOrGeneProduct denotes VUR
T36 1658-1663 GeneOrGeneProduct denotes cases
T37 1664-1671 GeneOrGeneProduct denotes yielded
T38 1746-1750 GeneOrGeneProduct denotes weak
T39 1766-1772 GeneOrGeneProduct denotes UP III
T40 1781-1784 GeneOrGeneProduct denotes VUR
T41 1824-1829 GeneOrGeneProduct denotes cases
T42 1864-1868 GeneOrGeneProduct denotes weak
T43 1889-1893 GeneOrGeneProduct denotes lack
T44 1911-1917 GeneOrGeneProduct denotes simple
T45 1962-1970 GeneOrGeneProduct denotes missense
T46 2037-2040 GeneOrGeneProduct denotes VUR
T47 2073-2077 GeneOrGeneProduct denotes weak
T48 2083-2090 GeneOrGeneProduct denotes factors
T49 2140-2144 GeneOrGeneProduct denotes fact
T50 2153-2163 GeneOrGeneProduct denotes truncation
T51 2173-2178 GeneOrGeneProduct denotes shift
T52 2179-2188 GeneOrGeneProduct denotes mutations
T53 2219-2222 GeneOrGeneProduct denotes VUR
T54 2257-2264 GeneOrGeneProduct denotes finding
T55 2284-2289 GeneOrGeneProduct denotes pairs
T56 2293-2299 GeneOrGeneProduct denotes UP III
T57 2300-2308 GeneOrGeneProduct denotes knockout
T58 2309-2313 GeneOrGeneProduct denotes mice
T59 2314-2319 GeneOrGeneProduct denotes yield
T60 2347-2350 GeneOrGeneProduct denotes VUR
T61 2403-2409 GeneOrGeneProduct denotes raises
T62 2431-2436 GeneOrGeneProduct denotes major
T63 2447-2456 GeneOrGeneProduct denotes mutations
T64 2495-2501 GeneOrGeneProduct denotes lethal

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 0-4 GeneOrGeneProduct denotes Lack
T2 8-13 GeneOrGeneProduct denotes major
T3 54-75 GeneOrGeneProduct denotes vesicoureteral reflux
T4 137-158 GeneOrGeneProduct denotes vesicoureteral reflux
T5 160-163 GeneOrGeneProduct denotes VUR
T6 293-298 GeneOrGeneProduct denotes young
T7 586-611 GeneOrGeneProduct denotes integral membrane protein
T8 647-650 GeneOrGeneProduct denotes VUR
T9 759-762 GeneOrGeneProduct denotes VUR
T10 845-848 GeneOrGeneProduct denotes VUR
T11 852-862 GeneOrGeneProduct denotes polymerase
T12 863-868 GeneOrGeneProduct denotes chain
T13 1162-1165 GeneOrGeneProduct denotes VUR
T14 1214-1217 GeneOrGeneProduct denotes VUR
T15 1246-1250 GeneOrGeneProduct denotes race
T16 1298-1301 GeneOrGeneProduct denotes VUR
T17 1425-1428 GeneOrGeneProduct denotes VUR
T18 1439-1443 GeneOrGeneProduct denotes SNP1
T19 1447-1452 GeneOrGeneProduct denotes UP Ia
T20 1523-1529 GeneOrGeneProduct denotes UP III
T21 1616-1619 GeneOrGeneProduct denotes VUR
T22 1746-1750 GeneOrGeneProduct denotes weak
T23 1766-1772 GeneOrGeneProduct denotes UP III
T24 1781-1784 GeneOrGeneProduct denotes VUR
T25 1864-1868 GeneOrGeneProduct denotes weak
T26 1889-1893 GeneOrGeneProduct denotes lack
T27 2037-2040 GeneOrGeneProduct denotes VUR
T28 2073-2077 GeneOrGeneProduct denotes weak
T29 2140-2144 GeneOrGeneProduct denotes fact
T30 2219-2222 GeneOrGeneProduct denotes VUR
T31 2293-2299 GeneOrGeneProduct denotes UP III
T32 2300-2308 GeneOrGeneProduct denotes knockout
T33 2347-2350 GeneOrGeneProduct denotes VUR
T34 2431-2436 GeneOrGeneProduct denotes major
T35 2495-2501 GeneOrGeneProduct denotes lethal

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 54-75 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux D014718
T2 94-101 DiseaseOrPhenotypicFeature denotes disease D004194
T3 137-158 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux D014718
T4 160-163 DiseaseOrPhenotypicFeature denotes VUR D014718
T5 343-362 DiseaseOrPhenotypicFeature denotes hereditary diseases D030342
T6 379-390 DiseaseOrPhenotypicFeature denotes nephropathy DISEASE
T7 416-439 DiseaseOrPhenotypicFeature denotes end-stage renal failure D007676
T8 647-650 DiseaseOrPhenotypicFeature denotes VUR D014718
T9 655-669 DiseaseOrPhenotypicFeature denotes hydronephrosis D006869
T10 759-762 DiseaseOrPhenotypicFeature denotes VUR D014718
T11 845-848 DiseaseOrPhenotypicFeature denotes VUR D014718
T12 1162-1165 DiseaseOrPhenotypicFeature denotes VUR D014718
T13 1214-1217 DiseaseOrPhenotypicFeature denotes VUR D014718
T14 1298-1301 DiseaseOrPhenotypicFeature denotes VUR D014718
T15 1425-1428 DiseaseOrPhenotypicFeature denotes VUR D014718
T16 1616-1619 DiseaseOrPhenotypicFeature denotes VUR D014718
T17 1781-1784 DiseaseOrPhenotypicFeature denotes VUR D014718
T18 2037-2040 DiseaseOrPhenotypicFeature denotes VUR D014718
T19 2127-2134 DiseaseOrPhenotypicFeature denotes disease D004194
T20 2219-2222 DiseaseOrPhenotypicFeature denotes VUR D014718
T21 2347-2350 DiseaseOrPhenotypicFeature denotes VUR D014718
T22 2368-2382 DiseaseOrPhenotypicFeature denotes hydronephrosis D006869
T23 2387-2401 DiseaseOrPhenotypicFeature denotes neonatal death D066087

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 586-611 GeneOrGeneProduct denotes integral membrane protein
T2 1246-1250 GeneOrGeneProduct denotes race
T3 1439-1443 GeneOrGeneProduct denotes SNP1
T4 1447-1452 GeneOrGeneProduct denotes UP Ia
T5 1523-1529 GeneOrGeneProduct denotes UP III
T6 1766-1772 GeneOrGeneProduct denotes UP III
T7 2140-2144 GeneOrGeneProduct denotes fact
T8 2293-2299 GeneOrGeneProduct denotes UP III

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 54-75 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux 0006007
T2 137-158 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux 0006007
T3 160-163 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T5 343-362 DiseaseOrPhenotypicFeature denotes hereditary diseases 0003847
T6 379-390 DiseaseOrPhenotypicFeature denotes nephropathy 0005240
T7 416-439 DiseaseOrPhenotypicFeature denotes end-stage renal failure 0004375
T8 647-650 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T10 655-669 DiseaseOrPhenotypicFeature denotes hydronephrosis 0005510
T11 759-762 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T13 845-848 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T15 1162-1165 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T17 1214-1217 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T19 1298-1301 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T21 1425-1428 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T23 1616-1619 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T25 1781-1784 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T27 2037-2040 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T29 2219-2222 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T31 2347-2350 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007
T33 2368-2382 DiseaseOrPhenotypicFeature denotes hydronephrosis 0005510

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 54-75 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux D014718
T2 94-101 DiseaseOrPhenotypicFeature denotes disease D004194
T3 137-158 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux D014718
T4 160-163 DiseaseOrPhenotypicFeature denotes VUR D014718
T5 170-189 DiseaseOrPhenotypicFeature denotes hereditary disorder DISEASE
T6 343-362 DiseaseOrPhenotypicFeature denotes hereditary diseases D030342
T7 379-390 DiseaseOrPhenotypicFeature denotes nephropathy DISEASE
T8 416-439 DiseaseOrPhenotypicFeature denotes end-stage renal failure D007676
T9 647-650 DiseaseOrPhenotypicFeature denotes VUR D014718
T10 655-669 DiseaseOrPhenotypicFeature denotes hydronephrosis D006869
T11 759-762 DiseaseOrPhenotypicFeature denotes VUR D014718
T12 845-848 DiseaseOrPhenotypicFeature denotes VUR D014718
T13 1162-1165 DiseaseOrPhenotypicFeature denotes VUR D014718
T14 1214-1217 DiseaseOrPhenotypicFeature denotes VUR D014718
T15 1298-1301 DiseaseOrPhenotypicFeature denotes VUR D014718
T16 1425-1428 DiseaseOrPhenotypicFeature denotes VUR D014718
T17 1616-1619 DiseaseOrPhenotypicFeature denotes VUR D014718
T18 1781-1784 DiseaseOrPhenotypicFeature denotes VUR D014718
T19 2037-2040 DiseaseOrPhenotypicFeature denotes VUR D014718
T20 2127-2134 DiseaseOrPhenotypicFeature denotes disease D004194
T21 2219-2222 DiseaseOrPhenotypicFeature denotes VUR D014718
T22 2347-2350 DiseaseOrPhenotypicFeature denotes VUR D014718
T23 2368-2382 DiseaseOrPhenotypicFeature denotes hydronephrosis D006869
T24 2387-2401 DiseaseOrPhenotypicFeature denotes neonatal death D066087

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 54-75 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux D014718
T2 137-158 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux D014718
T3 160-163 DiseaseOrPhenotypicFeature denotes VUR D014718
T4 170-189 DiseaseOrPhenotypicFeature denotes hereditary disorder DISEASE
T5 343-362 DiseaseOrPhenotypicFeature denotes hereditary diseases D030342
T6 379-390 DiseaseOrPhenotypicFeature denotes nephropathy DISEASE
T7 416-439 DiseaseOrPhenotypicFeature denotes end-stage renal failure D007676
T8 647-650 DiseaseOrPhenotypicFeature denotes VUR D014718
T9 655-669 DiseaseOrPhenotypicFeature denotes hydronephrosis D006869
T10 759-762 DiseaseOrPhenotypicFeature denotes VUR D014718
T11 845-848 DiseaseOrPhenotypicFeature denotes VUR D014718
T12 1162-1165 DiseaseOrPhenotypicFeature denotes VUR D014718
T13 1214-1217 DiseaseOrPhenotypicFeature denotes VUR D014718
T14 1298-1301 DiseaseOrPhenotypicFeature denotes VUR D014718
T15 1425-1428 DiseaseOrPhenotypicFeature denotes VUR D014718
T16 1616-1619 DiseaseOrPhenotypicFeature denotes VUR D014718
T17 1781-1784 DiseaseOrPhenotypicFeature denotes VUR D014718
T18 2037-2040 DiseaseOrPhenotypicFeature denotes VUR D014718
T19 2219-2222 DiseaseOrPhenotypicFeature denotes VUR D014718
T20 2347-2350 DiseaseOrPhenotypicFeature denotes VUR D014718
T21 2368-2382 DiseaseOrPhenotypicFeature denotes hydronephrosis D006869
T22 2387-2401 DiseaseOrPhenotypicFeature denotes neonatal death D066087

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 29-34 OrganismTaxon denotes human
T2 513-518 OrganismTaxon denotes mouse
T3 753-758 OrganismTaxon denotes human
T4 801-809 OrganismTaxon denotes patients
T5 1302-1310 OrganismTaxon denotes patients
T6 2044-2050 OrganismTaxon denotes humans
T7 2223-2231 OrganismTaxon denotes patients
T8 2309-2313 OrganismTaxon denotes mice
T9 2505-2511 OrganismTaxon denotes humans

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T8 2293-2299 GeneOrGeneProduct denotes UP III
T7 2140-2144 GeneOrGeneProduct denotes fact
T6 1766-1772 GeneOrGeneProduct denotes UP III
T5 1523-1529 GeneOrGeneProduct denotes UP III
T4 1447-1452 GeneOrGeneProduct denotes UP Ia
T3 1439-1443 GeneOrGeneProduct denotes SNP1
T2 1246-1250 GeneOrGeneProduct denotes race
T1 586-611 GeneOrGeneProduct denotes integral membrane protein
T22 2387-2401 DiseaseOrPhenotypicFeature denotes neonatal death D066087
T21 2368-2382 DiseaseOrPhenotypicFeature denotes hydronephrosis D006869
T20 2347-2350 DiseaseOrPhenotypicFeature denotes VUR D014718
T19 2219-2222 DiseaseOrPhenotypicFeature denotes VUR D014718
T18 2037-2040 DiseaseOrPhenotypicFeature denotes VUR D014718
T17 1781-1784 DiseaseOrPhenotypicFeature denotes VUR D014718
T16 1616-1619 DiseaseOrPhenotypicFeature denotes VUR D014718
T15 1425-1428 DiseaseOrPhenotypicFeature denotes VUR D014718
T14 1298-1301 DiseaseOrPhenotypicFeature denotes VUR D014718
T13 1214-1217 DiseaseOrPhenotypicFeature denotes VUR D014718
T12 1162-1165 DiseaseOrPhenotypicFeature denotes VUR D014718
T11 845-848 DiseaseOrPhenotypicFeature denotes VUR D014718
T10 759-762 DiseaseOrPhenotypicFeature denotes VUR D014718
T9 655-669 DiseaseOrPhenotypicFeature denotes hydronephrosis D006869
T38901 647-650 DiseaseOrPhenotypicFeature denotes VUR D014718
T24720 416-439 DiseaseOrPhenotypicFeature denotes end-stage renal failure D007676
T15958 379-390 DiseaseOrPhenotypicFeature denotes nephropathy DISEASE
T47820 343-362 DiseaseOrPhenotypicFeature denotes hereditary diseases D030342
T45975 170-189 DiseaseOrPhenotypicFeature denotes hereditary disorder DISEASE
T69412 160-163 DiseaseOrPhenotypicFeature denotes VUR D014718
T83773 137-158 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux D014718
T79755 54-75 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux D014718
T92547 2505-2511 OrganismTaxon denotes humans
T89180 2309-2313 OrganismTaxon denotes mice
T55980 2223-2231 OrganismTaxon denotes patients
T60905 2044-2050 OrganismTaxon denotes humans
T10024 1302-1310 OrganismTaxon denotes patients
T12206 801-809 OrganismTaxon denotes patients
T8583 753-758 OrganismTaxon denotes human
T60470 513-518 OrganismTaxon denotes mouse
T55288 29-34 OrganismTaxon denotes human
T56764 1566-1575 SequenceVariant denotes Pro154Ala
T6432 1495-1502 SequenceVariant denotes Ala7Val

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
15200408-9#9#13#gene6625 1439-1443 gene6625 denotes SNP1
15200408-9#186#189#diseaseC0042580 1616-1619 diseaseC0042580 denotes VUR
9#13#gene6625186#189#diseaseC0042580 15200408-9#9#13#gene6625 15200408-9#186#189#diseaseC0042580 associated_with SNP1,VUR

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 1495-1502 ProteinMutation:p|SUB|A|7|V denotes Ala7Val
T2 1566-1575 ProteinMutation:p|SUB|P|154|A denotes Pro154Ala

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1439-1443 gene:6625 denotes SNP1
T1 1616-1619 disease:C0042580 denotes VUR
R1 T0 T1 associated_with SNP1,VUR