Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_provenance.
- NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_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." NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_provenance.
- NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_assertion evidence source_evidence_curated NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_provenance.
- NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_assertion SIO_000772 20818383 NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_provenance.
- NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_assertion wasDerivedFrom uniprot-20130724 NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_provenance.
- NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_assertion wasGeneratedBy ECO_0000218 NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4211.RA6SV8vQh0qqIvj-Ju7OjK3an3zMhNb21QM4TpIJvo_L4130_provenance.