Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_assertion> ?p ?o ?g. }
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- NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_assertion type Assertion NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_head.
- NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_assertion description "[The MTHFR 677C > T polymorphism may be a susceptibility factor for epilepsy, and its higher frequency in women with epilepsy may contribute to the increased risk of malformation in children of women with epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_provenance.
- NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_assertion evidence source_evidence_literature NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_provenance.
- NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_assertion SIO_000772 17904392 NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_provenance.
- NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_assertion wasDerivedFrom lhgdn-20090331 NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_provenance.
- NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_assertion wasGeneratedBy ECO_0000203 NP229697.RAD0O5DZQZkES6D8dA1gt-iV3w0I7-QR0_7phZObUR4g4130_provenance.