Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_assertion> ?p ?o ?g. }
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- NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_assertion type Assertion NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_head.
- NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_assertion wasGeneratedBy ECO_0000203 NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_provenance.
- NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_assertion wasDerivedFrom lhgdn-20090331 NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_provenance.
- NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_assertion SIO_000772 12771268 NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_provenance.
- NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_assertion evidence source_evidence_literature NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_provenance.
- NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_assertion description "[A novel F318C substitution alters a highly conserved residue in a predicted repeat domain of LGI1 which may participate in the development of the " autosomal dominant partial epilepsy with auditory features " phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_provenance.