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- source_evidence_literature type ECO_0000212 NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_provenance.
- NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_assertion description "[To investigate this further, a new cohort of women with epilepsy has been identified from maternity hospital records and genotyped for polymorphisms in MTHFR, serine hydroxymethyl transferase (SHMT1), methionine synthase (MTR) and methionine synthase reductase (MTRR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_provenance.
- NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_assertion evidence source_evidence_literature NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_provenance.
- NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_assertion SIO_000772 17904392 NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_provenance.
- NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_assertion wasDerivedFrom gad-20150221 NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_provenance.
- NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_assertion wasGeneratedBy ECO_0000203 NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP130745.RAyqcAeVBbljn1CVaslu_5R98xH6PX_vfspZJbqLH_RHM130_provenance.