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- source_evidence_literature type ECO_0000212 NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP500454.RA1cC5sZqijGyYzz-9BS00U0HJDEevDlIygFOcCJTy68k130_provenance.