Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_assertion type Assertion NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_head.
- NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_assertion description "[Finally, discovery of a shared activation of the hypoxic response in pheochromocytomas with mutations in VHL and SDH genes and uncovering of a common JunB-mediated apoptosis defect in the major hereditary groups of pheochromocytoma have provided a mechanistic basis for the clinical similarities between these distinct syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_provenance.
- NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_assertion evidence source_evidence_literature NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_provenance.
- NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_assertion SIO_000772 16357557 NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_provenance.
- NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_assertion wasDerivedFrom befree-20140225 NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_provenance.
- NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_assertion wasGeneratedBy ECO_0000203 NP202525.RAgw4P3Nv6bh7praKf1L82Db_fkpNpN8l2kNASil40uHY130_provenance.