Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_provenance.
- NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_assertion wasGeneratedBy ECO_0000203 NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_provenance.
- NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_assertion wasDerivedFrom befree-20140225 NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_provenance.
- NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_assertion SIO_000772 16384941 NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_provenance.
- NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_assertion evidence source_evidence_literature NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_provenance.
- NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP493342.RA2NouiINJNH4K-SsGo4AoznEU5xOZmIOr4eP05czKma0130_provenance.