Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_assertion> ?p ?o ?g. }
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- NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_assertion type Assertion NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_head.
- NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_assertion description "[A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_provenance.
- NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_assertion evidence source_evidence_literature NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_provenance.
- NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_assertion SIO_000772 20850105 NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_provenance.
- NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_assertion wasDerivedFrom befree-20140225 NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_provenance.
- NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_assertion wasGeneratedBy ECO_0000203 NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_provenance.