Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_provenance.
- NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_assertion description "[In a group of 121 case families (mother, father, and proband with DS and AVSD) and 122 control families (mother, father, and proband with DS and no CHD), tag SNPs were genotyped in and around five folate pathway genes: 5,10-methylenetetrahyrdofolate reductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR), cystathionine beta-synthase (CBS), and the reduced folate carrier (SLC19A1, RFC1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_provenance.
- NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_assertion evidence source_evidence_literature NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_provenance.
- NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_assertion SIO_000772 20718043 NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_provenance.
- NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_assertion wasDerivedFrom befree-2016 NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_provenance.
- NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_assertion wasGeneratedBy ECO_0000203 NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_provenance.
- befree-2016 importedOn "2016-02-19" NP833451.RAuOxdOJmJx7l7wjzq-Pa9DnGTDWk3PUJv7Y1nfJqdQlk130_provenance.