Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP905008.RAp5gLLI9bLhUfK8kCcGvMF_CTpt_wRg8DJ_s44iZNcLY#assertion> ?p ?o ?g. }
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- assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion evidence source_evidence_curated provenance.
- assertion SIO_000772 12000816 provenance.
- assertion wasDerivedFrom CTD_human provenance.
- assertion wasGeneratedBy ECO_0000218 provenance.