Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance.
- NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion description "[Mutations in PDE6A and the PDE6B genes lead to autosomal recessive (ar) forms of retinitis pigmentosa (RP) in human and to the homologous disease in dogs, designated generalised progressive retinal atrophy (gPRA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance.
- NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion evidence source_evidence_literature NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance.
- NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion SIO_000772 10782214 NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance.
- NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion wasDerivedFrom befree-20140225 NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance.
- NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_assertion wasGeneratedBy ECO_0000203 NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP703425.RACDvw9d0y87d6ffz8KOOUvXuxwOnJSYRMVId40Cy2zVE130_provenance.