Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_provenance.
- NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_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." NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_provenance.
- NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_assertion evidence source_evidence_literature NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_provenance.
- NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_assertion SIO_000772 20718043 NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_provenance.
- NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_assertion wasDerivedFrom befree-20140225 NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_provenance.
- NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_assertion wasGeneratedBy ECO_0000203 NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP356913.RAuFlh1cX0hijoKDncINq35UOFc5ASAaTA3VNsyLOjUUQ130_provenance.