Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_provenance.
- NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_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." NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_provenance.
- NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_assertion evidence source_evidence_literature NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_provenance.
- NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_assertion SIO_000772 17904392 NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_provenance.
- NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_assertion wasDerivedFrom befree-20140225 NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_provenance.
- NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_assertion wasGeneratedBy ECO_0000203 NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP508709.RAhFNh6ZfrJoaYLvNSv7bc3RZRQ97QSO1H42A3GmDYZk4130_provenance.