Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_provenance.
- NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_assertion description "[These results expand the phenotypic spectrum associated with PAX2 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract as part of papillorenal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_provenance.
- NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_assertion evidence source_evidence_literature NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_provenance.
- NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_assertion SIO_000772 24676634 NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_provenance.
- NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_assertion wasDerivedFrom befree-20150227 NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_provenance.
- NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_assertion wasGeneratedBy ECO_0000203 NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP609354.RAdvSNz8TYJ7gKZpyQpYnr0t2UeNl_Tvhvy_wlWg6ZdGU130_provenance.