Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_assertion> ?p ?o ?g. }
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- NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_assertion type Assertion NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_head.
- NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_assertion description "[In one of the patients, the PRKAR1A gene responsible for Carney Complex and the KCNJ2 gene causal for Andersen syndrome are deleted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_provenance.
- NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_assertion evidence source_evidence_literature NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_provenance.
- NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_assertion SIO_000772 22166941 NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_provenance.
- NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_assertion wasDerivedFrom befree-20150227 NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_provenance.
- NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_assertion wasGeneratedBy ECO_0000203 NP522342.RAQOCf_egRTa623lVSIS35wrbst9dVwuL36d0y1RcLrII130_provenance.