Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_provenance.
- NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_assertion description "[Using fluorescent connexin fusion proteins, we show that the mutation induces a transport defect similar to that found for the Vohwinkel syndrome mutation p.Asp66His.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_provenance.
- NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_assertion evidence source_evidence_literature NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_provenance.
- NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_assertion SIO_000772 17993581 NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_provenance.
- NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_assertion wasDerivedFrom befree-20140225 NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_provenance.
- NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_assertion wasGeneratedBy ECO_0000203 NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP824352.RAq5H7710U-SaYSN_d7TDhqgkZHSIq4myTHMpR7ClfyTA130_provenance.