Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_provenance.
- NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_assertion description "[Chromosome 17q21-23 harbors genes for platelet glycoprotein IIIa and angiotensin-converting enzyme (ACE), which are polymorphic for alleles Pl(A2) and ACE 'D.' These alleles have been independently and often associated with ischemic coronary artery disease (CAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_provenance.
- NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_assertion evidence source_evidence_literature NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_provenance.
- NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_assertion SIO_000772 11545752 NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_provenance.
- NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_assertion wasDerivedFrom befree-20150227 NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_provenance.
- NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_assertion wasGeneratedBy ECO_0000203 NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP518078.RAyg0W2gHt0FejJocMV6eN13E_cZhfUj6WR2-rmtQi_M0130_provenance.