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- source_evidence_literature type ECO_0000212 NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_provenance.
- NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_assertion description "[In conclusion, HDC rs17740607 polymorphism is at least a partial loss-of-function variant and acts as a protective factor against CHF, which provides novel highlights for investigating the contribution of CHF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_provenance.
- NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_assertion evidence source_evidence_literature NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_provenance.
- NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_assertion SIO_000772 25846768 NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_provenance.
- NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_assertion wasDerivedFrom befree-2016 NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_provenance.
- NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_assertion wasGeneratedBy ECO_0000203 NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1276168.RAtb2MpIDrNv7bxuXXCIPQhq3xc0k3Hme9TW6AsIg-Fkk130_provenance.