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- source_evidence_literature type ECO_0000212 NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_provenance.
- NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_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." NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_provenance.
- NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_assertion evidence source_evidence_literature NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_provenance.
- NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_assertion SIO_000772 21252495 NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_provenance.
- NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_assertion wasDerivedFrom befree-20150227 NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_provenance.
- NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_assertion wasGeneratedBy ECO_0000203 NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_provenance.