Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_provenance.
- NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_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." NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_provenance.
- NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_assertion evidence source_evidence_literature NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_provenance.
- NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_assertion SIO_000772 21252495 NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_provenance.
- NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_assertion wasDerivedFrom befree-20140225 NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_provenance.
- NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_assertion wasGeneratedBy ECO_0000203 NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_provenance.