Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_assertion type Assertion NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_head.
- NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_assertion description "[The following frequencies (patients v controls), odds ratios (ORs), and confidence intervals (CIs) of single risk factors were found: Lp(a) >30 mg/dL (26.4% v 4.7%; OR/CI, 7.2/3.8 to 13.8; P <.0001), FV G1691A (20.2% v 4%; OR/CI, 6/2.97 to 12.1; P <.0001), protein C deficiency (6% v 0.67%; OR/CI, 9.5/2 to 44.6; P =.001), PT G20210A (6% v 1.3%; OR/CI, 4.7/1.4 to 15.6; P =.01), and the MTHFR TT677 genotype (23.6% v 10.4%; OR/CI, 2.4/1.53 to 4.5; P <.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_provenance.
- NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_assertion evidence source_evidence_literature NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_provenance.
- NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_assertion SIO_000772 10572079 NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_provenance.
- NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_assertion wasDerivedFrom befree-20150227 NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_provenance.
- NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_assertion wasGeneratedBy ECO_0000203 NP575768.RA2m3T-n1b1dcwZGRcFT8es_j4tw6ES3UrzLWMTMbrv9I130_provenance.