Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_provenance.
- NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_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." NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_provenance.
- NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_assertion evidence source_evidence_literature NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_provenance.
- NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_assertion SIO_000772 17904392 NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_provenance.
- NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_assertion wasDerivedFrom gad-20150221 NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_provenance.
- NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_assertion wasGeneratedBy ECO_0000203 NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP130719.RAPKjHvYXLZGXBgcAdoI8PVYG9EdbvsaAb6Z4LlTk1rZM130_provenance.