Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_provenance.
- NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_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." NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_provenance.
- NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_assertion evidence source_evidence_curated NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_provenance.
- NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_assertion SIO_000772 20818383 NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_provenance.
- NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_assertion wasDerivedFrom uniprot-2016 NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_provenance.
- NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_assertion wasGeneratedBy ECO_0000218 NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6352.RAQTCDTphc9gci22ozv-6B302uXU0iKOa6akAklaxb7J4130_provenance.