Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_assertion> ?p ?o ?g. }
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- NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_assertion type Assertion NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_head.
- NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_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." NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_provenance.
- NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_assertion evidence source_evidence_literature NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_provenance.
- NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_assertion SIO_000772 11420577 NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_provenance.
- NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_assertion wasDerivedFrom befree-2016 NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_provenance.
- NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_assertion wasGeneratedBy ECO_0000203 NP321671.RAQWGSrhZx0ekpVFubfd9JQLjH5MfoMSdHiTm8mEhHeRE130_provenance.