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- source_evidence_literature type ECO_0000212 NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_provenance.
- NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_assertion wasGeneratedBy ECO_0000203 NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_provenance.
- NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_assertion wasDerivedFrom befree-20150227 NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_provenance.
- NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_assertion SIO_000772 19349604 NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_provenance.
- NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_assertion evidence source_evidence_literature NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_provenance.
- NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_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." NP266619.RAcrLhF6L9YPVIz-UwZa4lyj_ujs-p_WEn7DZ_XDcGG5M130_provenance.