Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_assertion> ?p ?o ?g. }
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- NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_assertion type Assertion NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_head.
- NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_assertion description "[In addition, autosomal recessive mutations in the erythroid-specific mitochondrial transporter SLC25A38 and glutaredoxin 5 (GLRX5) have recently been identified in SA patients with isolated erythroid phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_provenance.
- NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_assertion evidence source_evidence_literature NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_provenance.
- NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_assertion SIO_000772 21252495 NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_provenance.
- NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_assertion wasDerivedFrom befree-2016 NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_provenance.
- NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_assertion wasGeneratedBy ECO_0000203 NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_provenance.