Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_provenance.
- NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_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." NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_provenance.
- NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_assertion evidence source_evidence_curated NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_provenance.
- NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_assertion SIO_000772 20818383 NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_provenance.
- NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_assertion wasDerivedFrom uniprot-20150221 NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_provenance.
- NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_assertion wasGeneratedBy ECO_0000218 NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_provenance.