Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_provenance.
- befree-2016 importedOn "2016-02-19" NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_provenance.
- NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_assertion wasGeneratedBy ECO_0000203 NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_provenance.
- NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_assertion wasDerivedFrom befree-2016 NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_provenance.
- NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_assertion SIO_000772 21943668 NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_provenance.
- NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_assertion evidence source_evidence_literature NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_provenance.
- NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_assertion description "[Heterozygous loss of the RPS14 gene on 5q leads to activation of p53 in the erythroid lineage and the macrocytic anemia characteristic of the 5q-syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926039.RAduWLrwScdMGn9N-vn9tz4qv23W9wGXAg0IvscNV-EgA130_provenance.