Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_assertion> ?p ?o ?g. }
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- NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_assertion type Assertion NP4341.RA0kP4RGq0Hp6jhs1Ll_z1k6QASREBuKVVl4DhaqW8UHE130_head.
- 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.