Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_assertion> ?p ?o ?g. }
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- NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_assertion type Assertion NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_head.
- NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_assertion wasGeneratedBy ECO_0000203 NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_provenance.
- NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_assertion wasDerivedFrom befree-20140225 NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_provenance.
- NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_assertion SIO_000772 17525480 NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_provenance.
- NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_assertion evidence source_evidence_literature NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_provenance.
- NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_assertion description "[An intriguing hypothesis proposes that mutations of RET, NF1, VHL, or SDH predispose to hereditary pheochromocytoma/ paraganglioma by causing defective apoptotic culling of cells that would normally be destroyed during embryogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247382.RAXXWaWxwVUsRJtXtFRQ908DI6p6Evq8xS3dWmDpWlKJg130_provenance.