Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_provenance.
- NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_assertion description "[The skin disease erythrokeratoderma variabilis (EKV) has been shown to be associated with mutations in GJB3 and GJB4 encoding connexin (Cx)31 and Cx30.3, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_provenance.
- NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_assertion evidence source_evidence_literature NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_provenance.
- NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_assertion SIO_000772 16297190 NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_provenance.
- NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_assertion wasDerivedFrom befree-2016 NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_provenance.
- NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_assertion wasGeneratedBy ECO_0000203 NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_provenance.
- befree-2016 importedOn "2016-02-19" NP523202.RAUtPSRMZKVopi12463dmfqeeMiEO9ELrm-SWL3smBvlo130_provenance.