Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_provenance.
- NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_assertion description "[Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a common autosomal recessive disorder caused by mutations in the steroid 21-hydroxylase gene (CYP21A2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_provenance.
- NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_assertion evidence source_evidence_literature NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_provenance.
- NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_assertion SIO_000772 23073904 NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_provenance.
- NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_assertion wasDerivedFrom befree-2016 NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_provenance.
- NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_assertion wasGeneratedBy ECO_0000203 NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1021737.RA52XmMisdFI7POBwj9aJF9O-eYjAln5hGWsrz3rk7eJs130_provenance.