Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_assertion> ?p ?o ?g. }
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- NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_assertion type Assertion NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_head.
- NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_assertion description "[The results revealed a lower carrier frequency of the DDX58 rs3205166 G allele in DEN than in HCs and a higher frequency of the DDX58 rs669260 T/C genotype in DHF than in DF cases (P = 0.043, OR with 95 % CI 3.358 [1.038-10.861]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_provenance.
- NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_assertion evidence source_evidence_literature NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_provenance.
- NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_assertion SIO_000772 25850761 NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_provenance.
- NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_assertion wasDerivedFrom befree-2016 NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_provenance.
- NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_assertion wasGeneratedBy ECO_0000203 NP1276405.RAWp3Vmt9bSNmjbM9oGA15rCnMOP4PO979OJwhSX76bpA130_provenance.