Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_provenance.
- NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_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." NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_provenance.
- NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_assertion evidence source_evidence_literature NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_provenance.
- NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_assertion SIO_000772 17904392 NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_provenance.
- NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_assertion wasDerivedFrom gad-20150221 NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_provenance.
- NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_assertion wasGeneratedBy ECO_0000203 NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_provenance.
- gad-20150221 importedOn "2015-02-21" NP151987.RArlrTBK9WCW7cAUOyQAtcjA96X_1Sq_yXYjJY0xHN0_E130_provenance.