Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_provenance.
- NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_assertion wasGeneratedBy ECO_0000218 NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_provenance.
- NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_assertion wasDerivedFrom uniprot-20150221 NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_provenance.
- NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_assertion SIO_000772 23542697 NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_provenance.
- NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_assertion evidence source_evidence_curated NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_provenance.
- NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_assertion description "[Study of families with focal epilepsy that were too small for conventional clinical diagnosis with FFEVF identified DEPDC5 mutations in approximately 12% of families (10/82).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397.RAdWDT7fw2RLAAJtFzLtuL81oHS7tzXV3LWcVm0WJ3jCg130_provenance.