Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.
- NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_assertion wasGeneratedBy ECO_0000218 NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.
- NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_assertion wasDerivedFrom uniprot-2016 NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.
- NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_assertion SIO_000772 9529364 NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.
- NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_assertion evidence source_evidence_curated NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.
- NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_assertion description "[Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.