Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_provenance.
- NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_assertion description "[First, we used SNaPshot assay to genotype seven 3'UTR SNPs in 537 ESCC cases and 608 normal controls in a Chinese Han population and found that SNP rs6573 in 3'UTR of RAS-related proteins (RAP1A) was significantly associated with ESCC risk [P = 0.02, odds ratio (OR) = 0.43; 95% confidence interval (CI): 0.21-0.91] and pathologic stage (P = 0.03, OR = 1.89; 95% CI: 1.06-3.36).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_provenance.
- NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_assertion evidence source_evidence_literature NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_provenance.
- NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_assertion SIO_000772 22859270 NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_provenance.
- NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_assertion wasDerivedFrom befree-20140225 NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_provenance.
- NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_assertion wasGeneratedBy ECO_0000203 NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP441298.RA-Fh_YPBmaQWVedpLoEruNaYWfoOJ7Wl1wEaXpXmlxVc130_provenance.