Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_provenance.
- befree-20150227 importedOn "2015-02-27" NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_provenance.
- NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_assertion wasGeneratedBy ECO_0000203 NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_provenance.
- NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_assertion wasDerivedFrom befree-20150227 NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_provenance.
- NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_assertion SIO_000772 17847930 NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_provenance.
- NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_assertion evidence source_evidence_literature NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_provenance.
- NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_assertion description "[The IL1RN VNTR and the IKBL+ 738T > C gene polymorphisms were tested in 374 Caucasians: 151 cases with MI and 223 subjects with no history of coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491054.RAOt1BhMh-uN0H0G6CRciPHknfEHl47_wYe5ZmKSwcjas130_provenance.