Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_provenance.
- NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_assertion description "[To confirm this analysis, we cloned the illegitimate rearranged fragments from three samples, and the molecular and fluorescent in situ hybridization (FISH) analyses indicated the presence of chromosomal translocations juxtaposing a switch IGH region to sequences from chromosomes 11q13 (one PCL case) or 4p16.3 (two MM cases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_provenance.
- NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_assertion evidence source_evidence_literature NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_provenance.
- NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_assertion SIO_000772 9354676 NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_provenance.
- NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_assertion wasDerivedFrom befree-20140225 NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_provenance.
- NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_assertion wasGeneratedBy ECO_0000203 NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_provenance.
- befree-20140225 importedOn "2014-02-25" NP268245.RAgn7ZrMEUxI9e3ntDWrB5dr5FnOqFyjgKw4aS-UBCRas130_provenance.