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- source_evidence_literature type ECO_0000212 NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_provenance.
- NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_assertion description "[The data from this study show overall risk modulation of BCC by variant allele for T241M polymorphism in XRCC3 and gender-specific effect by E185Q polymorphism in NBS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_provenance.
- NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_assertion evidence source_evidence_literature NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_provenance.
- NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_assertion SIO_000772 16501254 NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_provenance.
- NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_assertion wasDerivedFrom befree-2016 NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_provenance.
- NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_assertion wasGeneratedBy ECO_0000203 NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_provenance.
- befree-2016 importedOn "2016-02-19" NP537407.RAHifzkwAmm1EFw8TiY4-Ojx3blhexlnr4gEsJJY39fJg130_provenance.