Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance.
- NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_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." NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance.
- NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_assertion evidence source_evidence_literature NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance.
- NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_assertion SIO_000772 17904392 NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance.
- NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_assertion wasDerivedFrom gad-20130706 NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance.
- NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_assertion wasGeneratedBy ECO_0000203 NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP84273.RAZiFJOP5wMLZCMPZUop1u9V3GBdrhIyXxQ4vyx1Ux5Mk130_provenance.