Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_assertion> ?p ?o ?g. }
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- NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_assertion type Assertion NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_head.
- NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_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." NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_provenance.
- NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_assertion evidence source_evidence_literature NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_provenance.
- NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_assertion SIO_000772 8796880 NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_provenance.
- NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_assertion wasDerivedFrom befree-20150227 NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_provenance.
- NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_assertion wasGeneratedBy ECO_0000203 NP523469.RAhsaix1Fc7bn1u3YhcGc3sVFsD2nDp3CE7YcTB4v-6_o130_provenance.