Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_provenance.
- NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_assertion description "[Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_provenance.
- NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_assertion evidence source_evidence_literature NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_provenance.
- NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_assertion SIO_000772 20507940 NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_provenance.
- NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_assertion wasDerivedFrom gad-20150221 NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_provenance.
- NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_assertion wasGeneratedBy ECO_0000203 NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP177239.RAO0njdi8SP17XMRzknO8tbQCgv_lAN3KuI37_lpBSbJQ130_provenance.