Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_provenance.
- NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_assertion description "[Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_provenance.
- NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_assertion evidence source_evidence_curated NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_provenance.
- NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_assertion SIO_000772 23623389 NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_provenance.
- NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_assertion wasDerivedFrom uniprot-20130724 NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_provenance.
- NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_assertion wasGeneratedBy ECO_0000218 NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP2011.RACpOcojQOIZThKi3zWUve6io1STGqqSA7a41UCvHnD3M130_provenance.