Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_provenance.
- NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_assertion description "[Mutations in connexin 31 (GJB3) and connexin 30.3 (GJB4), implicated in previous reports of EKV, and connexin 26 (GJB2), implicated in palmoplantar keratoderma, were unlikely given the lack of shared homozygous haplotypes in the regions surrounding these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_provenance.
- NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_assertion evidence source_evidence_literature NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_provenance.
- NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_assertion SIO_000772 15668823 NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_provenance.
- NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_assertion wasDerivedFrom befree-2016 NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_provenance.
- NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_assertion wasGeneratedBy ECO_0000203 NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_provenance.
- befree-2016 importedOn "2016-02-19" NP477812.RAfLSs3sCTk0Ot27zXevPxGvX8Ur02O3WPPHARfANH5MA130_provenance.