Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_assertion> ?p ?o ?g. }
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- NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_assertion type Assertion NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_head.
- NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_assertion description "[Screening for C677T and A1298C MTHFR polymorphisms in patients with epilepsy and risk of hyperhomocysteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_provenance.
- NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_assertion evidence source_evidence_literature NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_provenance.
- NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_assertion SIO_000772 15970629 NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_provenance.
- NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_assertion wasDerivedFrom befree-2016 NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_provenance.
- NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_assertion wasGeneratedBy ECO_0000203 NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_provenance.