Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_provenance.
- befree-2016 importedOn "2016-02-19" NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_provenance.
- NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_assertion wasGeneratedBy ECO_0000203 NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_provenance.
- NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_assertion wasDerivedFrom befree-2016 NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_provenance.
- NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_assertion SIO_000772 19119257 NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_provenance.
- NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_assertion evidence source_evidence_literature NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_provenance.
- NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_assertion description "[Recent studies have shown that a klotho gene mutation is related to endothelial dysfunction, thrombosis, and arteriosclerosis, which are regarded as causes of vascular access dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP712035.RADG9jZvM5vUsUpF7O51MpV52YlUvHgVk0FNF6p9rQjgk130_provenance.