Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion> ?p ?o ?g. }
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- NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion type Assertion NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_head.
- NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_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." NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.
- NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion evidence source_evidence_literature NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.
- NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion SIO_000772 17904392 NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.
- NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion wasDerivedFrom gad-20130706 NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.
- NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion wasGeneratedBy ECO_0000203 NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance.