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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-84 Sentence denotes Genetic investigation of four meiotic genes in women with premature ovarian failure.
T2 85-95 Sentence denotes OBJECTIVE:
T3 96-326 Sentence denotes The goal of this study was to determine whether mutations of meiotic genes, such as disrupted meiotic cDNA (DMC1), MutS homolog (MSH4), MSH5, and S. cerevisiae homolog (SPO11), were associated with premature ovarian failure (POF).
T4 327-334 Sentence denotes DESIGN:
T5 335-354 Sentence denotes Case-control study.
T6 355-363 Sentence denotes METHODS:
T7 364-473 Sentence denotes Blood sampling, karyotype, hormonal dosage, ultrasound, and ovarian biopsy were carried out on most patients.
T8 474-625 Sentence denotes However, the main outcome measure was the sequencing of genomic DNA from peripheral blood samples of 41 women with POF and 36 fertile women (controls).
T9 626-634 Sentence denotes RESULTS:
T10 635-826 Sentence denotes A single heterozygous missense mutation, substitution of a cytosine residue with thymidine in exon 2 of MSH5, was found in two Caucasian women in whom POF developed at 18 and 36 years of age.
T11 827-956 Sentence denotes This mutation resulted in replacement of a non-polar amino acid (proline) with a polar amino acid (serine) at position 29 (P29S).
T12 957-1049 Sentence denotes Neither 36 control women nor 39 other patients with POF possessed this genetic perturbation.
T13 1050-1231 Sentence denotes Another POF patient of African origin showed a homozygous nucleotide change in the tenth of DMC1 gene that led to an alteration of the amino acid composition of the protein (M200V).
T14 1232-1244 Sentence denotes CONCLUSIONS:
T15 1245-1522 Sentence denotes The symptoms of infertility observed in the DMC1 homozygote mutation carrier and in both patients with a heterozygous substitution in exon 2 of the MSH5 gene provide indirect evidence of the role of genes involved in meiotic recombination in the regulation of ovarian function.
T16 1523-1595 Sentence denotes MSH5 and DMC1 mutations may be one explanation for POF, albeit uncommon.

LitCoin-entities-OrganismTaxon-PD

Id Subject Object Predicate Lexical cue db_id
T1 242-255 OrganismTaxon denotes S. cerevisiae NCBItxid:4932

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
4650 47-52 OrganismTaxon denotes women NCBITaxon:9606
4651 58-83 DiseaseOrPhenotypicFeature denotes premature ovarian failure MESH:D016649
4652 204-208 GeneOrGeneProduct denotes DMC1 NCBIGene:11144
4653 211-215 GeneOrGeneProduct denotes MutS NCBIGene:850545
4654 225-229 GeneOrGeneProduct denotes MSH4 NCBIGene:4438
4655 232-236 GeneOrGeneProduct denotes MSH5 NCBIGene:4439
4656 242-255 OrganismTaxon denotes S. cerevisiae NCBITaxon:4932
4657 265-270 GeneOrGeneProduct denotes SPO11 NCBIGene:856364
4658 294-319 DiseaseOrPhenotypicFeature denotes premature ovarian failure MESH:D016649
4659 321-324 DiseaseOrPhenotypicFeature denotes POF MESH:D016649
4660 464-472 OrganismTaxon denotes patients NCBITaxon:9606
4661 578-583 OrganismTaxon denotes women NCBITaxon:9606
4662 589-592 DiseaseOrPhenotypicFeature denotes POF MESH:D016649
4663 608-613 OrganismTaxon denotes women NCBITaxon:9606
4664 694-725 SequenceVariant denotes cytosine residue with thymidine DBSNP:rs2075789
4665 739-743 GeneOrGeneProduct denotes MSH5 NCBIGene:4439
4666 772-777 OrganismTaxon denotes women NCBITaxon:9606
4667 786-789 DiseaseOrPhenotypicFeature denotes POF MESH:D016649
4668 891-948 SequenceVariant denotes (proline) with a polar amino acid (serine) at position 29 DBSNP:rs2075789
4669 950-954 SequenceVariant denotes P29S DBSNP:rs2075789
4670 976-981 OrganismTaxon denotes women NCBITaxon:9606
4671 995-1003 OrganismTaxon denotes patients NCBITaxon:9606
4672 1009-1012 DiseaseOrPhenotypicFeature denotes POF MESH:D016649
4673 1058-1061 DiseaseOrPhenotypicFeature denotes POF MESH:D016649
4674 1062-1069 OrganismTaxon denotes patient NCBITaxon:9606
4675 1142-1146 GeneOrGeneProduct denotes DMC1 NCBIGene:11144
4676 1224-1229 SequenceVariant denotes M200V DBSNP:rs2227914
4677 1261-1272 DiseaseOrPhenotypicFeature denotes infertility MESH:D007247
4678 1289-1293 GeneOrGeneProduct denotes DMC1 NCBIGene:11144
4679 1334-1342 OrganismTaxon denotes patients NCBITaxon:9606
4680 1393-1397 GeneOrGeneProduct denotes MSH5 NCBIGene:4439
4681 1523-1527 GeneOrGeneProduct denotes MSH5 NCBIGene:4439
4682 1532-1536 GeneOrGeneProduct denotes DMC1 NCBIGene:11144
4683 1574-1577 DiseaseOrPhenotypicFeature denotes POF MESH:D016649

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T1 950-954 SequenceVariant denotes P29S
T2 1224-1229 SequenceVariant denotes M200V

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 126-135 GeneOrGeneProduct denotes determine
T2 144-153 GeneOrGeneProduct denotes mutations
T3 180-189 GeneOrGeneProduct denotes disrupted
T4 198-202 GeneOrGeneProduct denotes cDNA
T5 204-208 GeneOrGeneProduct denotes DMC1
T6 211-223 GeneOrGeneProduct denotes MutS homolog
T7 225-229 GeneOrGeneProduct denotes MSH4
T8 232-236 GeneOrGeneProduct denotes MSH5
T9 256-263 GeneOrGeneProduct denotes homolog
T10 265-270 GeneOrGeneProduct denotes SPO11
T11 335-339 GeneOrGeneProduct denotes Case
T12 355-362 GeneOrGeneProduct denotes METHODS
T13 391-399 GeneOrGeneProduct denotes hormonal
T14 452-455 GeneOrGeneProduct denotes out
T15 487-491 GeneOrGeneProduct denotes main
T16 657-665 GeneOrGeneProduct denotes missense
T17 666-674 GeneOrGeneProduct denotes mutation
T18 739-743 GeneOrGeneProduct denotes MSH5
T19 813-818 GeneOrGeneProduct denotes years
T20 832-840 GeneOrGeneProduct denotes mutation
T21 874-879 GeneOrGeneProduct denotes polar
T22 880-890 GeneOrGeneProduct denotes amino acid
T23 908-913 GeneOrGeneProduct denotes polar
T24 914-924 GeneOrGeneProduct denotes amino acid
T25 989-994 GeneOrGeneProduct denotes other
T26 1142-1146 GeneOrGeneProduct denotes DMC1
T27 1185-1195 GeneOrGeneProduct denotes amino acid
T28 1215-1222 GeneOrGeneProduct denotes protein
T29 1289-1293 GeneOrGeneProduct denotes DMC1
T30 1305-1313 GeneOrGeneProduct denotes mutation
T31 1314-1321 GeneOrGeneProduct denotes carrier
T32 1393-1397 GeneOrGeneProduct denotes MSH5
T33 1462-1483 GeneOrGeneProduct denotes meiotic recombination
T34 1491-1501 GeneOrGeneProduct denotes regulation
T35 1523-1527 GeneOrGeneProduct denotes MSH5
T36 1532-1536 GeneOrGeneProduct denotes DMC1
T37 1537-1546 GeneOrGeneProduct denotes mutations

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 180-189 GeneOrGeneProduct denotes disrupted
T2 198-202 GeneOrGeneProduct denotes cDNA
T3 204-208 GeneOrGeneProduct denotes DMC1
T4 211-223 GeneOrGeneProduct denotes MutS homolog
T5 225-229 GeneOrGeneProduct denotes MSH4
T6 232-236 GeneOrGeneProduct denotes MSH5
T7 256-263 GeneOrGeneProduct denotes homolog
T8 265-270 GeneOrGeneProduct denotes SPO11
T9 739-743 GeneOrGeneProduct denotes MSH5
T10 880-890 GeneOrGeneProduct denotes amino acid
T11 914-924 GeneOrGeneProduct denotes amino acid
T12 989-994 GeneOrGeneProduct denotes other
T13 1142-1146 GeneOrGeneProduct denotes DMC1
T14 1185-1195 GeneOrGeneProduct denotes amino acid
T15 1215-1222 GeneOrGeneProduct denotes protein
T16 1289-1293 GeneOrGeneProduct denotes DMC1
T17 1314-1321 GeneOrGeneProduct denotes carrier
T18 1393-1397 GeneOrGeneProduct denotes MSH5
T19 1462-1483 GeneOrGeneProduct denotes meiotic recombination
T20 1523-1527 GeneOrGeneProduct denotes MSH5
T21 1532-1536 GeneOrGeneProduct denotes DMC1

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 58-83 DiseaseOrPhenotypicFeature denotes premature ovarian failure D016649
T2 294-319 DiseaseOrPhenotypicFeature denotes premature ovarian failure D016649
T3 321-324 DiseaseOrPhenotypicFeature denotes POF D016649
T4 589-592 DiseaseOrPhenotypicFeature denotes POF D016649
T5 786-789 DiseaseOrPhenotypicFeature denotes POF D016649
T6 1009-1012 DiseaseOrPhenotypicFeature denotes POF D016649
T7 1058-1061 DiseaseOrPhenotypicFeature denotes POF D016649
T8 1261-1272 DiseaseOrPhenotypicFeature denotes infertility D007246
T9 1574-1577 DiseaseOrPhenotypicFeature denotes POF D016649

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 204-208 GeneOrGeneProduct denotes DMC1
T2 211-223 GeneOrGeneProduct denotes MutS homolog
T3 225-229 GeneOrGeneProduct denotes MSH4
T4 232-236 GeneOrGeneProduct denotes MSH5
T5 265-270 GeneOrGeneProduct denotes SPO11
T6 739-743 GeneOrGeneProduct denotes MSH5
T7 1142-1146 GeneOrGeneProduct denotes DMC1
T8 1289-1293 GeneOrGeneProduct denotes DMC1
T9 1393-1397 GeneOrGeneProduct denotes MSH5
T10 1462-1483 GeneOrGeneProduct denotes meiotic recombination
T11 1523-1527 GeneOrGeneProduct denotes MSH5
T12 1532-1536 GeneOrGeneProduct denotes DMC1

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 58-83 DiseaseOrPhenotypicFeature denotes premature ovarian failure 0005387|0001119
T3 294-319 DiseaseOrPhenotypicFeature denotes premature ovarian failure 0005387|0001119
T5 321-324 DiseaseOrPhenotypicFeature denotes POF 0001119|0005387
T7 589-592 DiseaseOrPhenotypicFeature denotes POF 0001119|0005387
T9 786-789 DiseaseOrPhenotypicFeature denotes POF 0001119|0005387
T11 1009-1012 DiseaseOrPhenotypicFeature denotes POF 0001119|0005387
T13 1058-1061 DiseaseOrPhenotypicFeature denotes POF 0001119|0005387
T15 1261-1272 DiseaseOrPhenotypicFeature denotes infertility 0005047
T16 1574-1577 DiseaseOrPhenotypicFeature denotes POF 0001119|0005387

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 58-83 DiseaseOrPhenotypicFeature denotes premature ovarian failure D016649
T2 294-319 DiseaseOrPhenotypicFeature denotes premature ovarian failure D016649
T3 321-324 DiseaseOrPhenotypicFeature denotes POF D016649
T4 589-592 DiseaseOrPhenotypicFeature denotes POF D016649
T5 786-789 DiseaseOrPhenotypicFeature denotes POF D016649
T6 1009-1012 DiseaseOrPhenotypicFeature denotes POF D016649
T7 1058-1061 DiseaseOrPhenotypicFeature denotes POF D016649
T8 1261-1272 DiseaseOrPhenotypicFeature denotes infertility D007246
T9 1574-1577 DiseaseOrPhenotypicFeature denotes POF D016649

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 58-83 DiseaseOrPhenotypicFeature denotes premature ovarian failure D016649
T2 294-319 DiseaseOrPhenotypicFeature denotes premature ovarian failure D016649
T3 321-324 DiseaseOrPhenotypicFeature denotes POF D016649
T4 589-592 DiseaseOrPhenotypicFeature denotes POF D016649
T5 786-789 DiseaseOrPhenotypicFeature denotes POF D016649
T6 1009-1012 DiseaseOrPhenotypicFeature denotes POF D016649
T7 1058-1061 DiseaseOrPhenotypicFeature denotes POF D016649
T8 1261-1272 DiseaseOrPhenotypicFeature denotes infertility D007246
T9 1574-1577 DiseaseOrPhenotypicFeature denotes POF D016649

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 694-702 ChemicalEntity denotes cytosine D003596|http://purl.obolibrary.org/obo/CHEBI_16040
T3 716-725 ChemicalEntity denotes thymidine http://purl.obolibrary.org/obo/CHEBI_17748
T4 870-890 ChemicalEntity denotes non-polar amino acid http://purl.obolibrary.org/obo/CHEBI_25588
T5 892-899 ChemicalEntity denotes proline http://purl.obolibrary.org/obo/CHEBI_26271|http://purl.obolibrary.org/obo/CHEBI_17203
T7 908-924 ChemicalEntity denotes polar amino acid http://purl.obolibrary.org/obo/CHEBI_26167
T8 926-932 ChemicalEntity denotes serine http://purl.obolibrary.org/obo/CHEBI_17822

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 47-52 OrganismTaxon denotes women
T2 242-255 OrganismTaxon denotes S. cerevisiae
T3 464-472 OrganismTaxon denotes patients
T4 578-583 OrganismTaxon denotes women
T5 608-613 OrganismTaxon denotes women
T6 772-777 OrganismTaxon denotes women
T7 976-981 OrganismTaxon denotes women
T8 995-1003 OrganismTaxon denotes patients
T9 1062-1069 OrganismTaxon denotes patient
T10 1334-1342 OrganismTaxon denotes patients

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T8 926-932 ChemicalEntity denotes serine http://purl.obolibrary.org/obo/CHEBI_17822
T7 908-924 ChemicalEntity denotes polar amino acid http://purl.obolibrary.org/obo/CHEBI_26167
T5 892-899 ChemicalEntity denotes proline http://purl.obolibrary.org/obo/CHEBI_17203|http://purl.obolibrary.org/obo/CHEBI_26271
T4 870-890 ChemicalEntity denotes non-polar amino acid http://purl.obolibrary.org/obo/CHEBI_25588
T3 716-725 ChemicalEntity denotes thymidine http://purl.obolibrary.org/obo/CHEBI_17748
T1 694-702 ChemicalEntity denotes cytosine http://purl.obolibrary.org/obo/CHEBI_16040|D003596
T12 1532-1536 GeneOrGeneProduct denotes DMC1
T11 1523-1527 GeneOrGeneProduct denotes MSH5
T10 1462-1483 GeneOrGeneProduct denotes meiotic recombination
T9 1393-1397 GeneOrGeneProduct denotes MSH5
T58508 1289-1293 GeneOrGeneProduct denotes DMC1
T31163 1142-1146 GeneOrGeneProduct denotes DMC1
T6 739-743 GeneOrGeneProduct denotes MSH5
T96018 265-270 GeneOrGeneProduct denotes SPO11
T77525 232-236 GeneOrGeneProduct denotes MSH5
T44146 225-229 GeneOrGeneProduct denotes MSH4
T2 211-223 GeneOrGeneProduct denotes MutS homolog
T18087 204-208 GeneOrGeneProduct denotes DMC1
T95522 1574-1577 DiseaseOrPhenotypicFeature denotes POF D016649
T26247 1261-1272 DiseaseOrPhenotypicFeature denotes infertility D007246
T23563 1058-1061 DiseaseOrPhenotypicFeature denotes POF D016649
T34418 1009-1012 DiseaseOrPhenotypicFeature denotes POF D016649
T94219 786-789 DiseaseOrPhenotypicFeature denotes POF D016649
T81840 589-592 DiseaseOrPhenotypicFeature denotes POF D016649
T32519 321-324 DiseaseOrPhenotypicFeature denotes POF D016649
T88253 294-319 DiseaseOrPhenotypicFeature denotes premature ovarian failure D016649
T10903 58-83 DiseaseOrPhenotypicFeature denotes premature ovarian failure D016649
T18079 1334-1342 OrganismTaxon denotes patients
T16276 1062-1069 OrganismTaxon denotes patient
T42203 995-1003 OrganismTaxon denotes patients
T14624 976-981 OrganismTaxon denotes women
T6032 772-777 OrganismTaxon denotes women
T34163 608-613 OrganismTaxon denotes women
T42225 578-583 OrganismTaxon denotes women
T81676 464-472 OrganismTaxon denotes patients
T46995 242-255 OrganismTaxon denotes S. cerevisiae
T86143 47-52 OrganismTaxon denotes women
T71839 1224-1229 SequenceVariant denotes M200V
T28524 950-954 SequenceVariant denotes P29S

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1523-1527 gene:4439 denotes MSH5
T1 1574-1577 disease:C0085215 denotes POF
T2 1532-1536 gene:11144 denotes DMC1
T3 1574-1577 disease:C0085215 denotes POF
T4 1532-1536 gene:283987 denotes DMC1
T5 1574-1577 disease:C0085215 denotes POF
R1 T0 T1 associated_with MSH5,POF
R2 T2 T3 associated_with DMC1,POF
R3 T4 T5 associated_with DMC1,POF

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
18166824-8#174#179#geners2227914 1224-1229 geners2227914 denotes M200V
18166824-8#8#11#diseaseC0085215 1058-1061 diseaseC0085215 denotes POF
18166824-8#8#11#diseaseC0025322 1058-1061 diseaseC0025322 denotes POF
174#179#geners22279148#11#diseaseC0085215 18166824-8#174#179#geners2227914 18166824-8#8#11#diseaseC0085215 associated_with M200V,POF
174#179#geners22279148#11#diseaseC0025322 18166824-8#174#179#geners2227914 18166824-8#8#11#diseaseC0025322 associated_with M200V,POF

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
18166824-1#129#133#gene4438 225-229 gene4438 denotes MSH4
18166824-1#169#174#gene23626 265-270 gene23626 denotes SPO11
18166824-1#198#223#diseaseC0085215 294-319 diseaseC0085215 denotes premature ovarian failure
18166824-1#198#223#diseaseC0025322 294-319 diseaseC0025322 denotes premature ovarian failure
18166824-1#225#228#diseaseC0085215 321-324 diseaseC0085215 denotes POF
18166824-1#225#228#diseaseC0025322 321-324 diseaseC0025322 denotes POF
18166824-1#198#223#diseaseC0085215 294-319 diseaseC0085215 denotes premature ovarian failure
18166824-1#198#223#diseaseC0025322 294-319 diseaseC0025322 denotes premature ovarian failure
18166824-1#225#228#diseaseC0085215 321-324 diseaseC0085215 denotes POF
18166824-1#225#228#diseaseC0025322 321-324 diseaseC0025322 denotes POF
18166824-10#0#4#gene4439 1523-1527 gene4439 denotes MSH5
18166824-10#9#13#gene11144 1532-1536 gene11144 denotes DMC1
18166824-10#51#54#diseaseC0085215 1574-1577 diseaseC0085215 denotes POF
18166824-10#51#54#diseaseC0025322 1574-1577 diseaseC0025322 denotes POF
18166824-10#51#54#diseaseC0085215 1574-1577 diseaseC0085215 denotes POF
18166824-10#51#54#diseaseC0025322 1574-1577 diseaseC0025322 denotes POF
129#133#gene4438198#223#diseaseC0085215 18166824-1#129#133#gene4438 18166824-1#198#223#diseaseC0085215 associated_with MSH4,premature ovarian failure
129#133#gene4438198#223#diseaseC0025322 18166824-1#129#133#gene4438 18166824-1#198#223#diseaseC0025322 associated_with MSH4,premature ovarian failure
129#133#gene4438225#228#diseaseC0085215 18166824-1#129#133#gene4438 18166824-1#225#228#diseaseC0085215 associated_with MSH4,POF
129#133#gene4438225#228#diseaseC0025322 18166824-1#129#133#gene4438 18166824-1#225#228#diseaseC0025322 associated_with MSH4,POF
129#133#gene4438198#223#diseaseC0085215 18166824-1#129#133#gene4438 18166824-1#198#223#diseaseC0085215 associated_with MSH4,premature ovarian failure
129#133#gene4438198#223#diseaseC0025322 18166824-1#129#133#gene4438 18166824-1#198#223#diseaseC0025322 associated_with MSH4,premature ovarian failure
129#133#gene4438225#228#diseaseC0085215 18166824-1#129#133#gene4438 18166824-1#225#228#diseaseC0085215 associated_with MSH4,POF
129#133#gene4438225#228#diseaseC0025322 18166824-1#129#133#gene4438 18166824-1#225#228#diseaseC0025322 associated_with MSH4,POF
169#174#gene23626198#223#diseaseC0085215 18166824-1#169#174#gene23626 18166824-1#198#223#diseaseC0085215 associated_with SPO11,premature ovarian failure
169#174#gene23626198#223#diseaseC0025322 18166824-1#169#174#gene23626 18166824-1#198#223#diseaseC0025322 associated_with SPO11,premature ovarian failure
169#174#gene23626225#228#diseaseC0085215 18166824-1#169#174#gene23626 18166824-1#225#228#diseaseC0085215 associated_with SPO11,POF
169#174#gene23626225#228#diseaseC0025322 18166824-1#169#174#gene23626 18166824-1#225#228#diseaseC0025322 associated_with SPO11,POF
169#174#gene23626198#223#diseaseC0085215 18166824-1#169#174#gene23626 18166824-1#198#223#diseaseC0085215 associated_with SPO11,premature ovarian failure
169#174#gene23626198#223#diseaseC0025322 18166824-1#169#174#gene23626 18166824-1#198#223#diseaseC0025322 associated_with SPO11,premature ovarian failure
169#174#gene23626225#228#diseaseC0085215 18166824-1#169#174#gene23626 18166824-1#225#228#diseaseC0085215 associated_with SPO11,POF
169#174#gene23626225#228#diseaseC0025322 18166824-1#169#174#gene23626 18166824-1#225#228#diseaseC0025322 associated_with SPO11,POF
0#4#gene443951#54#diseaseC0085215 18166824-10#0#4#gene4439 18166824-10#51#54#diseaseC0085215 associated_with MSH5,POF
0#4#gene443951#54#diseaseC0025322 18166824-10#0#4#gene4439 18166824-10#51#54#diseaseC0025322 associated_with MSH5,POF
0#4#gene443951#54#diseaseC0085215 18166824-10#0#4#gene4439 18166824-10#51#54#diseaseC0085215 associated_with MSH5,POF
0#4#gene443951#54#diseaseC0025322 18166824-10#0#4#gene4439 18166824-10#51#54#diseaseC0025322 associated_with MSH5,POF
9#13#gene1114451#54#diseaseC0085215 18166824-10#9#13#gene11144 18166824-10#51#54#diseaseC0085215 associated_with DMC1,POF
9#13#gene1114451#54#diseaseC0025322 18166824-10#9#13#gene11144 18166824-10#51#54#diseaseC0025322 associated_with DMC1,POF
9#13#gene1114451#54#diseaseC0085215 18166824-10#9#13#gene11144 18166824-10#51#54#diseaseC0085215 associated_with DMC1,POF
9#13#gene1114451#54#diseaseC0025322 18166824-10#9#13#gene11144 18166824-10#51#54#diseaseC0025322 associated_with DMC1,POF

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 950-954 ProteinMutation:p|SUB|P|29|S denotes P29S
T2 1224-1229 ProteinMutation:p|SUB|M|200|V denotes M200V