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- source_evidence_literature type ECO_0000212 NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_provenance.
- NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_assertion description "[We conclude that the mutated genotypes of the ScaI polymorphism are negatively associated with overt nephropathy, whereas the mutated genotypes of BstXI polymorphism are positively associated with microalbuminuria. hANP gene variants may exert a protecti]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_provenance.
- NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_assertion evidence source_evidence_literature NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_provenance.
- NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_assertion SIO_000772 11408388 NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_provenance.
- NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_assertion wasDerivedFrom gad-20150221 NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_provenance.
- NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_assertion wasGeneratedBy ECO_0000203 NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP81044.RAu83GJQlACsIkk8n6Qo2hB6YRMYTN880ZovXI2aYuUT0130_provenance.