Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance.
- NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_assertion description "[Moreover, the frequency of endothelin-1 Lys198Asn polymorphism was investigated with respect to the prevalence of several actual or historical endorgan damages (renal disorder, coronary artery disease, vascular events, vascular damage, and congestive heart failure) in hypertensive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance.
- NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_assertion evidence source_evidence_literature NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance.
- NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_assertion SIO_000772 18923236 NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance.
- NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_assertion wasDerivedFrom befree-2016 NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance.
- NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_assertion wasGeneratedBy ECO_0000203 NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance.
- befree-2016 importedOn "2016-02-19" NP698211.RA4livSNueNAhRubxIEPoUOqyNPAqLqwEJvTzfPJZflYo130_provenance.