Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_provenance.
- NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_provenance.
- NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_assertion evidence source_evidence_literature NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_provenance.
- NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_assertion SIO_000772 23759358 NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_provenance.
- NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_assertion wasDerivedFrom befree-2016 NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_provenance.
- NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_assertion wasGeneratedBy ECO_0000203 NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_provenance.