Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_provenance.
- NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_assertion wasGeneratedBy ECO_0000218 NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_provenance.
- NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_assertion wasDerivedFrom ctd_human-20150221 NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_provenance.
- NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_assertion SIO_000772 22466610 NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_provenance.
- NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_assertion evidence source_evidence_curated NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_provenance.
- NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_assertion description "[Three of the seven known UV(S)S cases carry mutations in the Cockayne syndrome genes ERCC8 or ERCC6 (also known as CSA and CSB, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13930.RAmWoFSMnnPM3SuOuCR8PEvg0kjNMMbw1ir77gkDeyoAg130_provenance.