Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_provenance.
- NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_assertion description "[The combination of homozygous MTHFR 677T and angiotensin II type-1 receptor 1166C variants confers the risk of small-vessel-associated ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_provenance.
- NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_assertion evidence source_evidence_literature NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_provenance.
- NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_assertion SIO_000772 17726226 NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_provenance.
- NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_assertion wasDerivedFrom befree-20150227 NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_provenance.
- NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_assertion wasGeneratedBy ECO_0000203 NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_provenance.
- befree-20150227 importedOn "2015-02-27" NP230357.RA3MsV_rtmdWkMgtKXPUfB8hSirq0tnTb60dpi_pIRhio130_provenance.