Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_provenance.
- befree-2016 importedOn "2016-02-19" NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_provenance.
- NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_assertion wasGeneratedBy ECO_0000203 NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_provenance.
- NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_assertion wasDerivedFrom befree-2016 NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_provenance.
- NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_assertion SIO_000772 17442773 NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_provenance.
- NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_assertion evidence source_evidence_literature NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_provenance.
- NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_assertion description "[Analysis of NUP98 allelic expression in AML and myelodysplastic syndrome showed loss of heterozygosity observed in 29% of the former and 8% of the latter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605333.RAuUGDJ3YwA7PeD7BBByF4KsBxYRWNy8Dp-Dt0Uxlsd-8130_provenance.