Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_assertion> ?p ?o ?g. }
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- NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_assertion type Assertion NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_head.
- NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_assertion description "[The purpose of the present study was to analyse these findings among the French population and to investigate whether common polymorphisms in genes of the folate and homocysteine pathway, including the MTHFR 677C > T, MTHFR 1298A > C, the methionine synthase (MTR) 2756A > G, the cystathionine beta-synthase (CBS) 844Ins68 and the reduced folate carrier (RFC-1) 80G > A polymorphisms, contribute to the risk of trisomy 21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_provenance.
- NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_assertion evidence source_evidence_literature NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_provenance.
- NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_assertion SIO_000772 16115349 NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_provenance.
- NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_assertion wasDerivedFrom gad-20130706 NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_provenance.
- NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_assertion wasGeneratedBy ECO_0000203 NP52262.RApHmk2uGqEoB2Ih3Tgg8HEYmlih113802ra2X_xXZJaw130_provenance.