Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_provenance.
- befree-2016 importedOn "2016-02-19" NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_provenance.
- NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_assertion wasGeneratedBy ECO_0000203 NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_provenance.
- NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_assertion wasDerivedFrom befree-2016 NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_provenance.
- NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_assertion SIO_000772 16724007 NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_provenance.
- NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_assertion evidence source_evidence_literature NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_provenance.
- NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_assertion description "[Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551490.RAJaW3R_cIUZknY35Rwp9-txr5M9hd_wsBbYsU88XWAOs130_provenance.