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- source_evidence_literature type ECO_0000212 NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_provenance.
- NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_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." NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_provenance.
- NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_assertion evidence source_evidence_literature NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_provenance.
- NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_assertion SIO_000772 11420577 NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_provenance.
- NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_assertion wasDerivedFrom befree-2016 NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_provenance.
- NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_assertion wasGeneratedBy ECO_0000203 NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_provenance.
- befree-2016 importedOn "2016-02-19" NP321672.RAnX6z5A0ouPcB4GwCsQYy-IteZL9NttuJ1kva6-xIaCE130_provenance.