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- source_evidence_literature type ECO_0000212 NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_provenance.
- NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_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." NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_provenance.
- NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_assertion evidence source_evidence_literature NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_provenance.
- NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_assertion SIO_000772 17904392 NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_provenance.
- NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_assertion wasDerivedFrom befree-2016 NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_provenance.
- NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_assertion wasGeneratedBy ECO_0000203 NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_provenance.
- befree-2016 importedOn "2016-02-19" NP632460.RAh8dthgoccYO3d2577Ra7OjXy7p4-9VmyjQ6O7zQEj6c130_provenance.