Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_provenance.
- NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_assertion description "[High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_provenance.
- NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_assertion evidence source_evidence_curated NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_provenance.
- NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_assertion SIO_000772 20818383 NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_provenance.
- NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_assertion wasDerivedFrom ctd_human-20150221 NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_provenance.
- NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_assertion wasGeneratedBy ECO_0000218 NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP15146.RA4eplY8IEL_CCl44dTTDC-PP2egmSTKHR_WmLBoOj-jc130_provenance.