Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_assertion> ?p ?o ?g. }
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- NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_assertion type Assertion NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_head.
- NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_assertion description "[C677T and A1298C MTHFR polymorphisms should be examined when assessing genetic risk factors of hyperhomocysteinemia in epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_provenance.
- NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_assertion evidence source_evidence_literature NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_provenance.
- NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_assertion SIO_000772 15970629 NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_provenance.
- NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_assertion wasDerivedFrom lhgdn-20090331 NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_provenance.
- NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_assertion wasGeneratedBy ECO_0000203 NP190146.RA88DnkilKiwa791GJomXeOgYjjTCPeIOhhRat8y4FxDU130_provenance.