Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_provenance.
- NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_assertion description "[Persons homozygous for haplotype 3, which is a common variant of the glucocorticoid receptor gene, had a more than 2-fold increased risk of myocardial infarction (hazard ratio, 2.1; 95% confidence interval, 1.13-4.07) and an almost 3-fold increased risk of coronary heart disease (hazard ratio, 2.6; 95% confidence interval, 1.40-4.81) compared with nonhomozygous persons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_provenance.
- NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_assertion evidence source_evidence_literature NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_provenance.
- NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_assertion SIO_000772 18195193 NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_provenance.
- NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_assertion wasDerivedFrom befree-20140225 NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_provenance.
- NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_assertion wasGeneratedBy ECO_0000203 NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP452387.RAGmEHxmuvR5hqn7XS8coI75V5-VN4KniXZe1IgnWaenY130_provenance.