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- source_evidence_literature type ECO_0000212 NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_provenance.
- NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_assertion description "[Along with SM22? induction in PHN, confirmed at both mRNA and protein levels, SM22? was also induced across a broad range of proteinuric diseases, including experimental animal models (puromycin aminonucleoside nephropathy, adriamycin nephropathy, passive nephrotoxic nephritis, and diet-induced obesity) and human diseases (collapsing glomerulopathy, diabetic nephropathy, classic focal segmental glomerulosclerosis, IgA nephropathy, minimal-change disease, membranous nephropathy, and membranoproliferative glomerulonephritis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_provenance.
- NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_assertion evidence source_evidence_literature NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_provenance.
- NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_assertion SIO_000772 21289056 NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_provenance.
- NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_assertion wasDerivedFrom befree-2016 NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_provenance.
- NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_assertion wasGeneratedBy ECO_0000203 NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_provenance.
- befree-2016 importedOn "2016-02-19" NP869746.RAvcSkd01jocB7dJnEbH6IzBGShsKj1JnITg-0VPYkxEc130_provenance.