Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_provenance.
- NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_assertion description "[The aim of the study was to assess the frequency of SNP896A/G in the Toll-like receptor (TLR) 4 gene and SNP1350T/C in the TLR2 gene in patients with acute myocardial infarction (AMI) and to analyse the association of these SNPs with risk factors for atherosclerosis and clinical aspects of AMI in a sample of the Croatian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_provenance.
- NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_assertion evidence source_evidence_literature NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_provenance.
- NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_assertion SIO_000772 22229967 NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_provenance.
- NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_assertion wasDerivedFrom befree-20140225 NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_provenance.
- NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_assertion wasGeneratedBy ECO_0000203 NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_provenance.
- befree-20140225 importedOn "2014-02-25" NP556003.RASvQAXaTVH4E6bNF7YPxlVKmDRf3mgsTxs2FrLdgD294130_provenance.