Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_assertion> ?p ?o ?g. }
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- NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_assertion type Assertion NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_head.
- NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_assertion description "[The CDKL5 gene has been implicated in the molecular etiology of early-onset intractable seizures with infantile spasms (IS), severe hypotonia and atypical Rett syndrome (RTT) features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_provenance.
- NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_assertion evidence source_evidence_literature NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_provenance.
- NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_assertion SIO_000772 19793311 NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_provenance.
- NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_assertion wasDerivedFrom befree-20150227 NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_provenance.
- NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_assertion wasGeneratedBy ECO_0000203 NP719301.RAfCJllrtNGxSRL0t7rg3LomTpW-d8xbxG5hwSyIfz1Ww130_provenance.