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- source_evidence_literature type ECO_0000212 NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_provenance.
- NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_assertion description "[Phylogenetic analysis of the S-polymerase gene sequences showed that 66.7% (36/54) of the patients were infected with genotype D (D1, D2, D3), 25.9% (14/54) with genotype A (A1, A2), 5.6% (3/54) with subgenotype C2, and 2% (1/54) with genotype E. A comparison of virological characteristics showed significant differences between genotypes A, C and D. The comparison between HBeAg status and the G1896A stop codon mutation in patients with genotype D revealed a relationship between HBV G1896A precore mutants and genotype D and hepatitis B e antigen (HBeAg) seroconversion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_provenance.
- NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_assertion evidence source_evidence_literature NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_provenance.
- NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_assertion SIO_000772 25626648 NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_provenance.
- NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_assertion wasDerivedFrom befree-2016 NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_provenance.
- NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_assertion wasGeneratedBy ECO_0000203 NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1258887.RApLJkeG-DNObeHMhoFexoVZgnhRq6FQz-dNlwF-FmrwY130_provenance.