Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_assertion type Assertion NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_head.
- NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_assertion description "[Susceptibility genes for two syndromes of idiopathic generalized epilepsies, the benign familial neonatal convulsions and juvenile myoclonic epilepsy, have been assigned to the chromosomal regions 20q13 (EBN1), 8q24 (EBN2) and 6p21 (EJM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_provenance.
- NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_assertion evidence source_evidence_literature NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_provenance.
- NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_assertion SIO_000772 8796880 NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_provenance.
- NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_assertion wasDerivedFrom befree-20140225 NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_provenance.
- NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_assertion wasGeneratedBy ECO_0000203 NP619258.RAV3xep70XeDeu8CEfglMw6K2zf1HiPEMx-F8yK0dMNTw130_provenance.