Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_provenance.
- NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_assertion description "[Based on the unique phenotype of the proband and on the presence of heterozygous females with neurocognitive/psychiatric ailments, this study describes the potential roles for ARX mutations in epilepsy and neuropsychiatric disease, underscoring the importance of ARX in interneuron development, cerebral electrical activity, cognition, and behavior.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_provenance.
- NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_assertion evidence source_evidence_literature NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_provenance.
- NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_assertion SIO_000772 21426321 NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_provenance.
- NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_assertion wasDerivedFrom befree-20150227 NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_provenance.
- NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_assertion wasGeneratedBy ECO_0000203 NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978088.RAf0Gv5kklq9SCZLMh_3psRe_dNoEMgKgSKa45LnTNaRU130_provenance.