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- source_evidence_literature type ECO_0000212 NP978159.RAIzbm7oYoPzTZfNrQsC-Em8kv6f1rY0NyDv-n_co_RnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978159.RAIzbm7oYoPzTZfNrQsC-Em8kv6f1rY0NyDv-n_co_RnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978159.RAIzbm7oYoPzTZfNrQsC-Em8kv6f1rY0NyDv-n_co_RnU130_provenance.
- NP978159.RAIzbm7oYoPzTZfNrQsC-Em8kv6f1rY0NyDv-n_co_RnU130_assertion description "[In addition, they might reflect that other phenotypic features associated with CDKL5 mutations (Rett-like features, infantile spasm) or ARX mutations (dystonia, spasticity) are more distinctive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978159.RAIzbm7oYoPzTZfNrQsC-Em8kv6f1rY0NyDv-n_co_RnU130_provenance.
- NP978159.RAIzbm7oYoPzTZfNrQsC-Em8kv6f1rY0NyDv-n_co_RnU130_assertion evidence source_evidence_literature NP978159.RAIzbm7oYoPzTZfNrQsC-Em8kv6f1rY0NyDv-n_co_RnU130_provenance.
- NP978159.RAIzbm7oYoPzTZfNrQsC-Em8kv6f1rY0NyDv-n_co_RnU130_assertion SIO_000772 19734009 NP978159.RAIzbm7oYoPzTZfNrQsC-Em8kv6f1rY0NyDv-n_co_RnU130_provenance.
- NP978159.RAIzbm7oYoPzTZfNrQsC-Em8kv6f1rY0NyDv-n_co_RnU130_assertion wasDerivedFrom befree-20150227 NP978159.RAIzbm7oYoPzTZfNrQsC-Em8kv6f1rY0NyDv-n_co_RnU130_provenance.
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- befree-20150227 importedOn "2015-02-27" NP978159.RAIzbm7oYoPzTZfNrQsC-Em8kv6f1rY0NyDv-n_co_RnU130_provenance.