Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_provenance.
- NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_assertion description "[Subsequently, kidneys from patients with congenital nephrotic syndrome of the Finnish type (CNF), presenting with heavy proteinuria, and Wilms' tumor tissue were studied for the corresponding expression pattern for evidence of dedifferentiation/persistence of a fetal expression pattern.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_provenance.
- NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_assertion evidence source_evidence_literature NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_provenance.
- NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_assertion SIO_000772 9438174 NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_provenance.
- NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_assertion wasDerivedFrom befree-20140225 NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_provenance.
- NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_assertion wasGeneratedBy ECO_0000203 NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP439040.RAwoBMJaRg8mGeLl7JtjN0tbwHMu7wvEL4fHZO_YKRmKQ130_provenance.