Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_provenance.
- NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_assertion description "[We have identified nine genetic variants associated with fasting proinsulin. Our findings illuminate the biology underlying glucose homeostasis and T2D development in humans and argue against a direct role of proinsulin in coronary artery disease pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_provenance.
- NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_assertion evidence source_evidence_literature NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_provenance.
- NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_assertion SIO_000772 21873549 NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_provenance.
- NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_assertion wasDerivedFrom gad-20130706 NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_provenance.
- NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_assertion wasGeneratedBy ECO_0000203 NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_provenance.
- gad-20130706 importedOn "2013-07-06" NP53309.RAQWepZmah3HeHifc67oztXTAmySD7pzlQW8UvcAbJwT0130_provenance.