Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_assertion> ?p ?o ?g. }
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- NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_assertion type Assertion NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_head.
- NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_assertion description "[To investigate this further, a new cohort of women with epilepsy has been identified from maternity hospital records and genotyped for polymorphisms in MTHFR, serine hydroxymethyl transferase (SHMT1), methionine synthase (MTR) and methionine synthase reductase (MTRR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_provenance.
- NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_assertion evidence source_evidence_literature NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_provenance.
- NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_assertion SIO_000772 17904392 NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_provenance.
- NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_assertion wasDerivedFrom befree-2016 NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_provenance.
- NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_assertion wasGeneratedBy ECO_0000203 NP632459.RA5U-BCxQ9UngO_fTfIH3bKOdi1yxtR9rvLzauTYPStBs130_provenance.