Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_assertion> ?p ?o ?g. }
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- NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_assertion type Assertion NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_head.
- NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_assertion description "[Caucasian patients (n = 255) treated at two German hospitals for intracranial aneurysms and local controls (n = 348) were genotyped for the following polymorphisms: methionine synthase (MTR) c.2756A-->G, methylenetetrahydrofolate reductase (MTHFR) c.677C-->T, MTHFR c.1298A-->C, cystathionine beta-synthase (CBS) c.844_855ins68, CBS c.833T-->C, dihydrofolate reductase (DHFR) c.594 + 59del19bp, glutathione S-transferase Omega-1 (GSTO1) c.428C-->A, reduced folate carrier 1 (RFC1) c.80G-->A and transcobalamin 2 (Tc2) c.776C-->G.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_provenance.
- NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_assertion evidence source_evidence_literature NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_provenance.
- NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_assertion SIO_000772 18799873 NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_provenance.
- NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_assertion wasDerivedFrom gad-20150221 NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_provenance.
- NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_assertion wasGeneratedBy ECO_0000203 NP126611.RAnmF_xGR-dxAyjn6sdD7g3GPO1Hmm84Wwy2aulX4iW8g130_provenance.