Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_assertion> ?p ?o ?g. }
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- NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_assertion type Assertion NP6952.RARzxIIi7XbWVuCWAExx8X0E5digiLHLIEgcoyOKJpbMM130_head.
- 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.