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- NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_assertion type Assertion NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_head.
- NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_assertion description "[We report a new neurodegenerative phenotype associated with a known ARX mutation and causing early abnormal neurodevelopment, a complex movement disorder, and early infantile epileptic encephalopathy with a suppression-burst pattern (Ohtahara syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_provenance.
- NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_assertion evidence source_evidence_literature NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_provenance.
- NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_assertion SIO_000772 19747203 NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_provenance.
- NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_assertion wasDerivedFrom befree-20140225 NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_provenance.
- NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_assertion wasGeneratedBy ECO_0000203 NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_provenance.