Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_provenance.
- NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_assertion wasGeneratedBy ECO_0000218 NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_provenance.
- NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_assertion wasDerivedFrom ctd_human-2016 NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_provenance.
- NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_assertion SIO_000772 16384941 NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_provenance.
- NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_assertion evidence source_evidence_curated NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_provenance.
- NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_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." NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_provenance.