Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_provenance.
- befree-2016 importedOn "2016-02-19" NP335876.RAnSMAJ11OmjqKnfHkWgnF-U9dlkjMJlrVTb_rNmMcCVc130_provenance.
- 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.