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- source_evidence_literature type ECO_0000212 NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_provenance.
- NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_assertion description "[Genetic variation at the AGT gene influences the risk of nephropathy in T2DM patients but not extent of DN severity, and thus represents a potential DN genetic susceptibility locus worthy of replication.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_provenance.
- NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_assertion evidence source_evidence_literature NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_provenance.
- NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_assertion SIO_000772 21421655 NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_provenance.
- NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_assertion wasDerivedFrom befree-20150227 NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_provenance.
- NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_assertion wasGeneratedBy ECO_0000203 NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP877478.RAXE6eBVV-fNGsgylxKJrSE359zxFuAPH729fudUx9ct0130_provenance.