Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_assertion type Assertion NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_head.
- NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_assertion wasGeneratedBy ECO_0000203 NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_provenance.
- NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_assertion wasDerivedFrom befree-2016 NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_provenance.
- NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_assertion SIO_000772 11702207 NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_provenance.
- NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_assertion evidence source_evidence_literature NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_provenance.
- NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_assertion description "[Retinitis pigmentosa 3 (RP3) is a progressive retinal degeneration due to mutations in the X-linked RPGR gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_provenance.