Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_provenance.
- NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_assertion description "[It has been suggested that people with the epsilon4 allele of the apolipoprotein E (apoE) polymorphism and the deletion (D) allele of the insertion (I/D) polymorphism of angiotensin-converting enzymes, are at a greater risk for coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_provenance.
- NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_assertion evidence source_evidence_literature NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_provenance.
- NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_assertion SIO_000772 11420577 NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_provenance.
- NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_assertion wasDerivedFrom befree-20140225 NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_provenance.
- NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_assertion wasGeneratedBy ECO_0000203 NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_provenance.
- befree-20140225 importedOn "2014-02-25" NP191487.RAmIrjDyCJpk16vdp6jtk5CfXGeTUlLJYcAExE8cKvAog130_provenance.