Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_provenance.
- NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_assertion wasGeneratedBy ECO_0000218 NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_provenance.
- NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_assertion wasDerivedFrom uniprot-2016 NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_provenance.
- NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_assertion SIO_000772 9888386 NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_provenance.
- NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_assertion evidence source_evidence_curated NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_provenance.
- NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_assertion description "[In this paper, we report the molecular characterization of seven unrelated kindreds native from Colombia and Brazil with CGD caused by gp91-phox deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10013.RAC1A_GEwrnDzkfmYLIUhCoLHvq3t7smGvHwT3HRCSLQQ130_provenance.