Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_assertion> ?p ?o ?g. }
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- NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_assertion type Assertion NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_head.
- NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_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." NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_provenance.
- NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_assertion evidence source_evidence_literature NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_provenance.
- NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_assertion SIO_000772 16115349 NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_provenance.
- NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_assertion wasDerivedFrom befree-20140225 NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_provenance.
- NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_assertion wasGeneratedBy ECO_0000203 NP163562.RA3gBafagF76sQrHBPaePCisEuWKnm2KvHpdq-P8HJO8I130_provenance.