Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP738696.RAFE1PDKrqSvYjSEOAT4fnFy8ib-THD0bWwvAMJK925OQ130_provenance.