Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_provenance.
- NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_assertion description "[A novel MECP2 mutation in a boy with neonatal encephalopathy and facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_provenance.
- NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_assertion evidence source_evidence_curated NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_provenance.
- NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_assertion SIO_000772 19559301 NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_provenance.
- NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_assertion wasDerivedFrom ctd_human-20150221 NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_provenance.
- NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_assertion wasGeneratedBy ECO_0000218 NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP21792.RAFWCldxDNk3qxid6XTsbk69vlKOrkK5Gi25sOgwcLpu4130_provenance.