Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_provenance.
- NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_assertion description "[Our data implicate that the genotypic variation at codon 311 of PON2 contributes to the susceptibility of CAD in the population of Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_provenance.
- NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_assertion evidence source_evidence_literature NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_provenance.
- NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_assertion SIO_000772 12433026 NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_provenance.
- NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_assertion wasDerivedFrom befree-20150227 NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_provenance.
- NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_assertion wasGeneratedBy ECO_0000203 NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP635269.RAvWvCy9JO_wJ70g_d353M5_1iFiFsMxTtwU4oxwZmOXo130_provenance.