Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_provenance.
- NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_assertion description "[Fusion of the nucleoporin gene, NUP98, and the putative RNA helicase gene, DDX10, by inversion 11 (p15q22) chromosome translocation in a patient with etoposide-related myelodysplastic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_provenance.
- NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_assertion evidence source_evidence_literature NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_provenance.
- NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_assertion SIO_000772 10830185 NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_provenance.
- NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_assertion wasDerivedFrom befree-2016 NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_provenance.
- NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_assertion wasGeneratedBy ECO_0000203 NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_provenance.
- befree-2016 importedOn "2016-02-19" NP285073.RAus39PDEeLSDhDUB_7kGsC3f1D3p3didyjKi_HB3tkjc130_provenance.