Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_assertion> ?p ?o ?g. }
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- NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_assertion type Assertion NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_head.
- NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_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." NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_provenance.
- NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_assertion evidence source_evidence_literature NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_provenance.
- NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_assertion SIO_000772 17904392 NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_provenance.
- NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_assertion wasDerivedFrom gad-20150221 NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_provenance.
- NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_assertion wasGeneratedBy ECO_0000203 NP113623.RA_p8UhKDkGqK4OdoVnGwK5E6olfFq3uBdEc7O4-YIgGE130_provenance.