Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_provenance.
- NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_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." NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_provenance.
- NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_assertion evidence source_evidence_literature NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_provenance.
- NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_assertion SIO_000772 19734009 NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_provenance.
- NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_assertion wasDerivedFrom befree-2016 NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_provenance.
- NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_assertion wasGeneratedBy ECO_0000203 NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_provenance.
- befree-2016 importedOn "2016-02-19" NP761545.RAfpcEnH3eauRaR_Oap65raMdTvM2aFGCnMa4zn1sWv5A130_provenance.