Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_assertion> ?p ?o ?g. }
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- NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_assertion type Assertion NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_head.
- NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_assertion wasGeneratedBy ECO_0000203 NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_provenance.
- NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_assertion wasDerivedFrom befree-20140225 NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_provenance.
- NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_assertion SIO_000772 17525480 NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_provenance.
- NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_assertion evidence source_evidence_literature NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_provenance.
- NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_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." NP221823.RAG3MT6JC2eiwWcKGytpspApZh76Tc4ZtOBK56LJH9ytA130_provenance.