Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_provenance.
- NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_assertion wasGeneratedBy ECO_0000203 NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_provenance.
- NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_assertion wasDerivedFrom befree-20140225 NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_provenance.
- NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_assertion SIO_000772 10767341 NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_provenance.
- NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_assertion evidence source_evidence_literature NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_provenance.
- NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_assertion description "[Identical mutations in the CSB gene associated with either Cockayne syndrome or the DeSanctis-cacchione variant of xeroderma pigmentosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP846183.RAt0AHyXnWfb3NW5SZSrMn9u5YoKUv4rmQjWKKCTDF2Wk130_provenance.