Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_provenance.
- NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_assertion description "[These results extend our previous observations and indicate that defects in XPCC cause Xeroderma pigmentosum group C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_provenance.
- NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_assertion evidence source_evidence_curated NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_provenance.
- NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_assertion SIO_000772 8298653 NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_provenance.
- NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_assertion wasDerivedFrom uniprot-20130724 NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_provenance.
- NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_assertion wasGeneratedBy ECO_0000218 NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP7136.RAHsqCF30v64CslDjj7aeGchxAnCtp4uNH6KKcordbXIw130_provenance.