Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_assertion> ?p ?o ?g. }
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- NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_assertion type Assertion NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_head.
- NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_assertion description "[The rs3024409 variant allele of F13A1 was associated with 1.66-fold increased risk of VTE, while the minor alleles of HABP2 rs6585234 and rs3862019, F2R rs253061 and rs153311, and PLAUR rs344782 were each associated with lower risk of VTE (hazard ratios in the range of 0.49-0.66).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_provenance.
- NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_assertion evidence source_evidence_literature NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_provenance.
- NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_assertion SIO_000772 19552680 NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_provenance.
- NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_assertion wasDerivedFrom befree-20140225 NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_provenance.
- NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_assertion wasGeneratedBy ECO_0000203 NP355062.RAd535YEPCykBHlk7XbDMMQ5fqI0af6lHiDafH5ctz4Qw130_provenance.