Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_provenance.
- NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_assertion description "[Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_provenance.
- NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_assertion evidence source_evidence_curated NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_provenance.
- NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_assertion SIO_000772 22325361 NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_provenance.
- NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_assertion wasDerivedFrom uniprot-2016 NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_provenance.
- NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_assertion wasGeneratedBy ECO_0000218 NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_provenance.