Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance.
- NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_assertion description "[Our results suggest that characteristic sequence motifs located at the FUS, EWS and CHOP breakpoint regions, including Alu and palindromic oligomer sequences, are involved in the mechanisms creating chromosomal translocations in MLS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance.
- NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_assertion evidence source_evidence_literature NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance.
- NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_assertion SIO_000772 18752119 NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance.
- NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_assertion wasDerivedFrom befree-2016 NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance.
- NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_assertion wasGeneratedBy ECO_0000203 NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance.
- befree-2016 importedOn "2016-02-19" NP690020.RAwJ0_23hgPHRNJjlhZaJTTiRgF3XU5sxGFAWf_4TVpA0130_provenance.