Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_assertion> ?p ?o ?g. }
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- NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_assertion type Assertion NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_head.
- NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_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." NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_provenance.
- NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_assertion evidence source_evidence_literature NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_provenance.
- NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_assertion SIO_000772 17904392 NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_provenance.
- NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_assertion wasDerivedFrom befree-20150227 NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_provenance.
- NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_assertion wasGeneratedBy ECO_0000203 NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_provenance.