Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_provenance.
- NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_assertion description "[The Tyr99Cys GUCA1A mutation has been previously shown to cause autosomal dominant progressive cone dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_provenance.
- NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_assertion evidence source_evidence_literature NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_provenance.
- NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_assertion SIO_000772 15953638 NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_provenance.
- NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_assertion wasDerivedFrom befree-2016 NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_provenance.
- NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_assertion wasGeneratedBy ECO_0000203 NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_provenance.
- befree-2016 importedOn "2016-02-19" NP499274.RA8IwTCRJ_MUQ2InjsqpPTQjhLtrDZIvfMPt7sSDKPzkg130_provenance.