Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_provenance.
- NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_assertion description "[Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_provenance.
- NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_assertion evidence source_evidence_curated NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_provenance.
- NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_assertion SIO_000772 23708187 NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_provenance.
- NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_assertion wasDerivedFrom ctd_human-2016 NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_provenance.
- NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_assertion wasGeneratedBy ECO_0000218 NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP33020.RA3G3W41mht-EmU39P2FsUKVYtO5S-uYW8U8ttS52ajQs130_provenance.