Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_assertion> ?p ?o ?g. }
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- NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_assertion type Assertion NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_head.
- NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_assertion wasGeneratedBy ECO_0000203 NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_provenance.
- NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_assertion wasDerivedFrom befree-20140225 NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_provenance.
- NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_assertion SIO_000772 18045948 NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_provenance.
- NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_assertion evidence source_evidence_literature NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_provenance.
- NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_assertion description "[Most PHEOs are sporadic, but a significant percentage (approximately 25%) may be found in patients with germline mutations of genes predisposing to the development of von Hippel-Lindau disease, neurofibromatosis 1, multiple endocrine neoplasia type 1 (MEN1) and 2 (MEN2), and the PGL/PHEOs syndrome, based on the described mutations of the genes for succinate dehydrogenase subunit D (SDHD), B (SDHB), and C (SDHC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776244.RAa2SJraswEoUHODkZDzpzvr6MEJgrmmdFND4jwPtS8nU130_provenance.