Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_assertion> ?p ?o ?g. }
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- NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_assertion type Assertion NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_head.
- NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_assertion description "[In conclusion, this case report of MEN 2A linked to a 634 RET mutation was peculiar by its revelation mode (1) hyperparathyroidism moreover linked to an adenoma and (2) associated with diabetes, mechanisms of which are probably multifactorial (familial type 2 diabetes, hypercalcemia, catecholamines excess).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_provenance.
- NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_assertion evidence source_evidence_literature NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_provenance.
- NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_assertion SIO_000772 18752792 NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_provenance.
- NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_assertion wasDerivedFrom befree-20140225 NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_provenance.
- NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_assertion wasGeneratedBy ECO_0000203 NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_provenance.