Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_provenance.
- NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_assertion description "[Mutations in genes of the nucleotide excision repair (NER) pathway are associated with diseases, such as xeroderma pigmentosum and Cockayne syndrome, that involve increased skin cancer and/or developmental and neurological symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_provenance.
- NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_assertion evidence source_evidence_literature NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_provenance.
- NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_assertion SIO_000772 21568835 NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_provenance.
- NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_assertion wasDerivedFrom befree-20140225 NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_provenance.
- NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_assertion wasGeneratedBy ECO_0000203 NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP327602.RACWo6ccPVt9r2o2F7cx0rzQMk3kefiJWwyszu5aDvpKE130_provenance.