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- source_evidence_literature type ECO_0000212 NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_provenance.
- NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_assertion description "[We examined the association between different polymorphisms frequently found in young patients with cryptogenic stroke [methylenetetrahydrofolate reductase (MTHFR) C677T, factor II (prothrombin) G20210A, factor V G1691A (Leiden), nitric oxide synthase 3 (NOS3) intron 4 VNTR, and apolipoprotein E (APOE) epsilon4 gene] in patients with a cerebral infarct caused by spontaneous cervical artery dissection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_provenance.
- NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_assertion evidence source_evidence_literature NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_provenance.
- NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_assertion SIO_000772 20446941 NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_provenance.
- NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_assertion wasDerivedFrom befree-2016 NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_provenance.
- NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_assertion wasGeneratedBy ECO_0000203 NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_provenance.
- befree-2016 importedOn "2016-02-19" NP810387.RAvdRt0VkMGEF39eGa2aAywUSOdszkLEJ0ggV9-DZHxEs130_provenance.