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- source_evidence_literature type ECO_0000212 NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_provenance.
- NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_assertion description "[Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), nucleotide excision repair (XPC-PAT, XPA-23G>A, ERCC1-19007T>C and XPD-L751Q), recombination (XRCC3-T241M) and alkylation damage reversal (MGMT-L84F) were tested for their potential role in the development of GC by using logistic regression models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_provenance.
- NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_assertion evidence source_evidence_literature NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_provenance.
- NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_assertion SIO_000772 20817763 NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_provenance.
- NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_assertion wasDerivedFrom befree-20140225 NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_provenance.
- NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_assertion wasGeneratedBy ECO_0000203 NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP276814.RAUdEj_CZ4KkfYL6U5dh0X0cIAgV-ntlphcMlCUTZfWYE130_provenance.