Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_provenance.
- NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_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." NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_provenance.
- NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_assertion evidence source_evidence_literature NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_provenance.
- NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_assertion SIO_000772 18752119 NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_provenance.
- NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_assertion wasDerivedFrom befree-2016 NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_provenance.
- NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_assertion wasGeneratedBy ECO_0000203 NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_provenance.
- befree-2016 importedOn "2016-02-19" NP690022.RAiRU53NoiSDLf7WljHXeVrvWI4p8XJpiTuWT6UJyifc4130_provenance.