Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance.
- NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_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." NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance.
- NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_assertion evidence source_evidence_literature NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance.
- NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_assertion SIO_000772 18752119 NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance.
- NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_assertion wasDerivedFrom befree-20150227 NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance.
- NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_assertion wasGeneratedBy ECO_0000203 NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP414164.RAgJSn6q7fpGXl2MTkOhgztEpkcJmclkw3EynpnUp9H4k130_provenance.