Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_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." NP582518.RAbi-gXTf7LgRvCmUAqvLd0mcyiAnp54GJnU5WTLCrFKc130_provenance.
- NP277957.RAsgWo_UsFq0usY9YBFQOpQwKarzr_llUVin15k8ALUnA130_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." NP277957.RAsgWo_UsFq0usY9YBFQOpQwKarzr_llUVin15k8ALUnA130_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.
- NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_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." NP611727.RA-0KPgbBNrD3U_cGA4RezCwrc4DpT76Bv4cUFZ7gvzqo130_provenance.
- NP611728.RA1i3GLOUpvUuTC_zii26TYHqL-x5lb6zVYfpcGrvaTkk130_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." NP611728.RA1i3GLOUpvUuTC_zii26TYHqL-x5lb6zVYfpcGrvaTkk130_provenance.
- NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_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." NP611726.RAfiWxPau15t-OBDGhK1XVuDTQ-G25DvaBsMJzxGdyrJc130_provenance.
- 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." provenance.
- 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." provenance.
- 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." provenance.
- NP611729.RArQfpCKo16zhv625Wkdus4Gjya9RCtzqaRGVj7pxQiTw130_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." NP611729.RArQfpCKo16zhv625Wkdus4Gjya9RCtzqaRGVj7pxQiTw130_provenance.