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- source_evidence_literature type ECO_0000212 NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_provenance.
- NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_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." NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_provenance.
- NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_assertion evidence source_evidence_literature NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_provenance.
- NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_assertion SIO_000772 17904392 NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_provenance.
- NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_assertion wasDerivedFrom lhgdn-20090331 NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_provenance.
- NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_assertion wasGeneratedBy ECO_0000203 NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP190145.RA-cgTMFnDQd62X079IsSdVCif_52U96j7wMIQ6lq7oQ4130_provenance.