Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_assertion> ?p ?o ?g. }
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- NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_assertion type Assertion NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_head.
- NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_assertion description "[Compared with the CC genotypes of each polymorphism, the associations of a slightly reduced risk of SCCHN with the variant genotypes of CT + TT of both polymorphisms were approaching statistical significance [Odds ratio (OR) = 0.90, 95% confidence interval (CI) = 0.76-1.08 for TERT-rs2736098 and OR = 0.86, 95% CI = 0.71-1.04 for CLPTM1L-rs401681, respectively].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_provenance.
- NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_assertion evidence source_evidence_literature NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_provenance.
- NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_assertion SIO_000772 20802237 NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_provenance.
- NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_assertion wasDerivedFrom befree-20140225 NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_provenance.
- NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_assertion wasGeneratedBy ECO_0000203 NP712615.RAFDeOITK6YvX7YKDjjyIc7ApKXig_Qrq4GDfsPIEfZn4130_provenance.