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- NP4223.RAb3q-LnGKENTL00eIqgLn3efBo9R8IZmD3V1qKAn2Sm0130_assertion type Assertion NP4223.RAb3q-LnGKENTL00eIqgLn3efBo9R8IZmD3V1qKAn2Sm0130_head.
- NP4223.RAb3q-LnGKENTL00eIqgLn3efBo9R8IZmD3V1qKAn2Sm0130_assertion wasGeneratedBy ECO_0000218 NP4223.RAb3q-LnGKENTL00eIqgLn3efBo9R8IZmD3V1qKAn2Sm0130_provenance.
- NP4223.RAb3q-LnGKENTL00eIqgLn3efBo9R8IZmD3V1qKAn2Sm0130_assertion wasDerivedFrom uniprot-20130724 NP4223.RAb3q-LnGKENTL00eIqgLn3efBo9R8IZmD3V1qKAn2Sm0130_provenance.
- NP4223.RAb3q-LnGKENTL00eIqgLn3efBo9R8IZmD3V1qKAn2Sm0130_assertion SIO_000772 20818383 NP4223.RAb3q-LnGKENTL00eIqgLn3efBo9R8IZmD3V1qKAn2Sm0130_provenance.
- NP4223.RAb3q-LnGKENTL00eIqgLn3efBo9R8IZmD3V1qKAn2Sm0130_assertion evidence source_evidence_curated NP4223.RAb3q-LnGKENTL00eIqgLn3efBo9R8IZmD3V1qKAn2Sm0130_provenance.
- NP4223.RAb3q-LnGKENTL00eIqgLn3efBo9R8IZmD3V1qKAn2Sm0130_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." NP4223.RAb3q-LnGKENTL00eIqgLn3efBo9R8IZmD3V1qKAn2Sm0130_provenance.