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Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.
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1 records shown · first 60Genetic Variants of RPL5 and RPL9 Genes among Saudi Patients Diagnosed with Thrombosis.
PMID 34483448 | PMCID PMC8385736 | DOI 10.5455/medarh.2021.75.188-193 · Medical archives (Sarajevo, Bosnia and Herzegovina) · 2021 · 5 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| variant | rs6604026 | “The RPL5 (L5) gene on intron 6 on chromosome 1p22, rs6604026 is associated with multiple sclerosis risk, whereas RPL9 (L9) on 8 exons on chromosome 4p14 has been documented so far as being an essential involvement in the proliferation of protein synthesized cells mostly by gene products.” | 0.90 | hgvs_regex_v1 |
| gene | RPL5 | “Genetic Variants of RPL5 and RPL9 Genes among Saudi Patients Diagnosed with Thrombosis.” | 0.98 | hgnc_dict_v1 |
| gene | RPL9 | “Genetic Variants of RPL5 and RPL9 Genes among Saudi Patients Diagnosed with Thrombosis.” | 0.98 | hgnc_dict_v1 |
| phenotype | multiple sclerosis | “The RPL5 (L5) gene on intron 6 on chromosome 1p22, rs6604026 is associated with multiple sclerosis risk, whereas RPL9 (L9) on 8 exons on chromosome 4p14 has been documented so far as being an essential involvement in the proliferation of protein synthesized cells mostly by gene products.” | 0.98 | phenotype_alias_lexicon_v2 |