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PMC:7295011 / 4881-5259 JSONTXT

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LitCovid-PMC-OGER-BB

Id Subject Object Predicate Lexical cue
T82 37-44 SO:0000704 denotes genetic
T83 61-67 PR:000004690 denotes BCL11A
T84 68-72 SO:0000704 denotes gene
T85 92-98 SO:0001026 denotes genome
T86 227-234 SO:0000704 denotes genetic
T87 271-279 GO:0065007 denotes modulate
T88 317-328 CL:0000740 denotes sickle cell
T31772 37-44 SO:0000704 denotes genetic
T50101 61-67 PR:000004690 denotes BCL11A
T63374 68-72 SO:0000704 denotes gene
T29873 92-98 SO:0001026 denotes genome
T83318 227-234 SO:0000704 denotes genetic
T2944 271-279 GO:0065007 denotes modulate
T77581 317-328 CL:0000740 denotes sickle cell

LitCovid-PD-FMA-UBERON

Id Subject Object Predicate Lexical cue fma_id
T8 68-72 Body_part denotes gene http://purl.org/sig/ont/fma/fma74402
T9 92-98 Body_part denotes genome http://purl.org/sig/ont/fma/fma84116
T10 140-150 Body_part denotes hemoglobin http://purl.org/sig/ont/fma/fma62293
T11 324-328 Body_part denotes cell http://purl.org/sig/ont/fma/fma68646

LitCovid-PubTator

Id Subject Object Predicate Lexical cue tao:has_database_id
110 61-67 Gene denotes BCL11A Gene:53335
120 301-312 Disease denotes thalassemia MESH:D013789

LitCovid-PD-MONDO

Id Subject Object Predicate Lexical cue mondo_id
T37 296-312 Disease denotes beta-thalassemia http://purl.obolibrary.org/obo/MONDO_0013517
T38 301-312 Disease denotes thalassemia http://purl.obolibrary.org/obo/MONDO_0000984
T39 317-337 Disease denotes sickle cell diseases http://purl.obolibrary.org/obo/MONDO_0011382

LitCovid-PD-CLO

Id Subject Object Predicate Lexical cue
T33 68-72 http://purl.obolibrary.org/obo/OGG_0000000002 denotes gene
T34 324-328 http://purl.obolibrary.org/obo/GO_0005623 denotes cell

LitCovid-PD-CHEBI

Id Subject Object Predicate Lexical cue chebi_id
T12 140-150 Chemical denotes hemoglobin http://purl.obolibrary.org/obo/CHEBI_35143
T13 296-300 Chemical denotes beta http://purl.obolibrary.org/obo/CHEBI_10545

LitCovid-sentences

Id Subject Object Predicate Lexical cue
T28 0-378 Sentence denotes In one example of how this can work, genetic variants in the BCL11A gene were associated by genome-wide association studies (GWAS) to fetal hemoglobin (HbF) production in the general population (Menzel et al., 2007), and these genetic variants were subsequently found to modulate the severity of beta-thalassemia and sickle cell diseases (Lettre et al., 2008; Uda et al., 2008).

2_test

Id Subject Object Predicate Lexical cue
32582302-17767159-33453884 210-214 17767159 denotes 2007
32582302-18667698-33453885 354-358 18667698 denotes 2008
32582302-18245381-33453886 372-376 18245381 denotes 2008

MyTest

Id Subject Object Predicate Lexical cue
32582302-17767159-33453884 210-214 17767159 denotes 2007
32582302-18667698-33453885 354-358 18667698 denotes 2008
32582302-18245381-33453886 372-376 18245381 denotes 2008