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- source_evidence_literature type ECO_0000212 NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_provenance.
- NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_assertion description "[Based on Cox regression and Kaplan-Meier analyses, statistically significant differences were noted in BRCA2 mutation carriers by health status in 3 SNPs: CC homozygosity at rs6505162 increased ovarian cancer risk (RR 2.77; p = 0.028; 95% CI, 1.11-6.9); heterozygote SNP carriers of rs11169571 had an approximately 2 fold increased risk for developing breast/ovarian cancer, whereas heterozygotes of the rs895819 SNP had an approximately 50% reduced risk for developing breast/ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_provenance.
- NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_assertion evidence source_evidence_literature NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_provenance.
- NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_assertion SIO_000772 19950226 NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_provenance.
- NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_assertion wasDerivedFrom befree-2016 NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_provenance.
- NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_assertion wasGeneratedBy ECO_0000203 NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_provenance.
- befree-2016 importedOn "2016-02-19" NP778537.RAiIi-aDaSdgh4N9WZnsp6ST-j9U8iva95RU3VnJkfuGA130_provenance.