Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_provenance.
- NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_assertion description "[The results demonstrate that NPHS1 and NPHS2 mutations are also present in Chinese sporadic NS patients, suggesting that genetic changes of nephrin and podocin may play pathogenetic roles in some patients with sporadic steroid resistant NS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_provenance.
- NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_assertion evidence source_evidence_literature NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_provenance.
- NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_assertion SIO_000772 17211152 NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_provenance.
- NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_assertion wasDerivedFrom gad-20130706 NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_provenance.
- NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_assertion wasGeneratedBy ECO_0000203 NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_provenance.
- gad-20130706 importedOn "2013-07-06" NP66053.RAUrivh46IFClOJS2NyNRkBcAEBK41MI8QUvcEOf4r3hw130_provenance.