Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_provenance.
- NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_assertion description "[The features of these are 1) late onset of seizures, 2) good response to ACTH therapy, 3) no significant abnormalities of brain except for agenesis of corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_provenance.
- NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_assertion evidence source_evidence_curated NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_provenance.
- NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_assertion SIO_000772 2169275 NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_provenance.
- NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_assertion wasDerivedFrom ctd_human-20150221 NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_provenance.
- NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_assertion wasGeneratedBy ECO_0000218 NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP26571.RAqdlwLag1cdoapEPvrlquNG9gNbuj8_85Tz5IJDwV2CU130_provenance.