Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP591989.RA-uClW-v4FTFS-xD3w43hRO-5aC1gl4rG7-8tCxu8sOg130_provenance.