Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_assertion> ?p ?o ?g. }
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- NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_assertion type Assertion NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_head.
- NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_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." NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_provenance.
- NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_assertion evidence source_evidence_literature NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_provenance.
- NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_assertion SIO_000772 20446941 NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_provenance.
- NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_assertion wasDerivedFrom befree-2016 NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_provenance.
- NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_assertion wasGeneratedBy ECO_0000203 NP810386.RAbHwUQRc4mY8KbrpopgyKbAoX9xLOrHxI8lk8hWl6HDE130_provenance.