Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_provenance.
- NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_assertion description "[Our findings support the contributory role of the II/I polymorphism in leptin gene in the pathogenesis of hypertension, and this role was more evident in Asians and for essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_provenance.
- NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_assertion evidence source_evidence_literature NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_provenance.
- NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_assertion SIO_000772 25475696 NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_provenance.
- NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_assertion wasDerivedFrom befree-2016 NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_provenance.
- NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_assertion wasGeneratedBy ECO_0000203 NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244877.RAoaC6NCUF_Cd43a2sdgPh2mwrJMn4pDnIVA3eqFBriNQ130_provenance.