Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_assertion> ?p ?o ?g. }
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- NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_assertion type Assertion NP1009197.RABLdsF5yTG_9JgONV4GPyRVumj1wcMURdfq95U7ML_ig130_head.
- 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.