Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_provenance.
- NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_assertion wasGeneratedBy ECO_0000203 NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_provenance.
- NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_assertion wasDerivedFrom befree-20140225 NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_provenance.
- NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_assertion SIO_000772 23144630 NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_provenance.
- NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_assertion evidence source_evidence_literature NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_provenance.
- NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_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." NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP890856.RAw_XtY_ugi-6pibSIFMRQN9BVFaR7Q6Nt_8jUD5GEFJo130_provenance.