Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_provenance.
- NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_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." NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_provenance.
- NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_assertion evidence source_evidence_curated NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_provenance.
- NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_assertion SIO_000772 24676634 NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_provenance.
- NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_assertion wasDerivedFrom uniprot-2016 NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_provenance.
- NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_assertion wasGeneratedBy ECO_0000218 NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7833.RATpZvGF8m636RoGMawLpl0zKgKC5o4wKIGUy8IAZgN0w130_provenance.