Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_provenance.
- NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_assertion wasGeneratedBy ECO_0000203 NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_provenance.
- NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_assertion wasDerivedFrom befree-20140225 NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_provenance.
- NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_assertion SIO_000772 15370538 NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_provenance.
- NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_assertion evidence source_evidence_literature NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_provenance.
- NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_assertion description "[Leber congenital amaurosis (LCA; estimated prevalence 1 : 50,000-100,000) is an early-onset inherited cause of childhood blindness characterized by a severe retinal dystrophy immediately after birth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP545964.RAQ5EQDTArAsvPAWVL1fTVYoqS9pqB0Ttm-Wks9zRvjzY130_provenance.