Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_assertion type Assertion NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_head.
- NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_assertion wasGeneratedBy ECO_0000203 NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_provenance.
- NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_assertion wasDerivedFrom befree-2016 NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_provenance.
- NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_assertion SIO_000772 19349604 NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_provenance.
- NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_assertion evidence source_evidence_literature NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_provenance.
- NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_assertion description "[Individuals with the p.R168X mutation and heterozygous for the BDNF polymorphism were also at an increased risk of seizure onset (hazard ratio 5.3, 95% confidence interval 1.6-17.7) compared with those homozygous for the wild-type BDNF allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP730830.RAg37Z7iPxf8DxOkiKKZNMGp2m5YaMUL-M6t2PVRHHk9A130_provenance.