Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP693746.RAjPM02JVpNfMC4SW_szt4OQ83x6GkLG99UQWE4xgTaII130_provenance.