Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_assertion> ?p ?o ?g. }
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- NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_assertion type Assertion NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_head.
- NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_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." NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_provenance.
- NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_assertion evidence source_evidence_literature NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_provenance.
- NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_assertion SIO_000772 12000816 NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_provenance.
- NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_assertion wasDerivedFrom gad-20130706 NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_provenance.
- NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_assertion wasGeneratedBy ECO_0000203 NP59235.RA54CBDUH5riF9gYnUcvMkpIgp769pPYKGYABnmPuxii0130_provenance.