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- source_evidence_literature type ECO_0000212 NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_provenance.
- NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_assertion description "[Our results offer more evidence that in patients with FH, NPHS2-R229Q predisposes to proteinuria and ESKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_provenance.
- NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_assertion evidence source_evidence_literature NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_provenance.
- NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_assertion SIO_000772 22228437 NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_provenance.
- NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_assertion wasDerivedFrom befree-20140225 NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_provenance.
- NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_assertion wasGeneratedBy ECO_0000203 NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP930980.RAE1e-IlYBxN0z35V7VozTdCZGdSxOUjtbfYtJnXs92Mw130_provenance.