Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_provenance.
- befree-2016 importedOn "2016-02-19" NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_provenance.
- NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_assertion wasGeneratedBy ECO_0000203 NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_provenance.
- NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_assertion wasDerivedFrom befree-2016 NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_provenance.
- NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_assertion SIO_000772 17442773 NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_provenance.
- NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_assertion evidence source_evidence_literature NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_provenance.
- NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_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." NP605328.RA9LEVuBk8ApQ2mgYqV3_nmLtFdim-n6jRgjzGpNPpdwc130_provenance.