Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_provenance.
- NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_assertion description "[After the adjustment for covariates, the carriers of minor D allele of RGS2-rs34717272 had an increased hypertension risk (DD+ID vs. II; odds ratio=1.19; 95% confidence interval, 1.04-1.35; P value after the Bonferroni correction=0.009 x 5=0.045).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_provenance.
- NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_assertion evidence source_evidence_literature NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_provenance.
- NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_assertion SIO_000772 18496125 NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_provenance.
- NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_assertion wasDerivedFrom gad-20130706 NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_provenance.
- NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_assertion wasGeneratedBy ECO_0000203 NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_provenance.
- gad-20130706 importedOn "2013-07-06" NP52259.RA7PkCdP5P8KAGZJEehrpqd5fm5uOkUKZ0HzVEvHDqX8U130_provenance.