Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_assertion> ?p ?o ?g. }
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- NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_assertion type Assertion NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_head.
- NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_assertion wasGeneratedBy ECO_0000203 NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_provenance.
- NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_assertion wasDerivedFrom befree-20150227 NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_provenance.
- NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_assertion SIO_000772 23144630 NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_provenance.
- NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_assertion evidence source_evidence_literature NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_provenance.
- NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_assertion description "[Heterozygous mutations in the PRPF31 gene cause autosomal dominant retinitis pigmentosa (adRP), a hereditary disorder leading to progressive blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881938.RAnQt9SDoPTMz9VgO51q5dcraTuxMhIzl3MkXz0mJ5CC4130_provenance.