Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_provenance.
- NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_assertion wasGeneratedBy ECO_0000203 NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_provenance.
- NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_assertion wasDerivedFrom befree-20150227 NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_provenance.
- NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_assertion SIO_000772 16384941 NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_provenance.
- NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_assertion evidence source_evidence_literature NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_provenance.
- NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_provenance.