Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_provenance.