Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_provenance.
- NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_assertion description "[In patients with CHF with CTI above 60% the number of carriers of genotypes with ET-1 8002A (AA and AG genotypes) increases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_provenance.
- NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_assertion evidence source_evidence_literature NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_provenance.
- NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_assertion SIO_000772 14729437 NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_provenance.
- NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_assertion wasDerivedFrom befree-20140225 NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_provenance.
- NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_assertion wasGeneratedBy ECO_0000203 NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP265621.RA5NfdF258lV48Z9dr9IC5vFzEVCAwnutKvB3JZ3TEnIE130_provenance.