Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_assertion> ?p ?o ?g. }
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- NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_assertion type Assertion NP16855.RAe3O3cbe4tWCxGNo4s9mmX0cxbWPU8jF-g4A3TUREAhw130_head.
- 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.