Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_provenance.
- NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_assertion description "[FOXG1B (forkhead box G1B) is a very intriguing candidate gene since it is known to promote neuronal progenitor proliferation and to suppress premature neurogenesis and its disruption is reported in a patient with postnatal microcephaly, corpus callosum agenesis, seizures, and severe mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_provenance.
- NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_assertion evidence source_evidence_curated NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_provenance.
- NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_assertion SIO_000772 18627055 NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_provenance.
- NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_assertion wasDerivedFrom ctd_human-20150221 NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_provenance.
- NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_assertion wasGeneratedBy ECO_0000218 NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP15087.RAXHRXwa6uOeowbFsH00PIMUz9F6aqHLI6TAf6kN9vgOY130_provenance.