Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_assertion> ?p ?o ?g. }
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- NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_assertion type Assertion NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_head.
- NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_assertion description "[These in vitro studies have demonstrated that the proliferation is characterized by a unique chromosomal abnormality, the 5q35bp usually associated with a t(2;5) translocation generating a fusion gene NPM/ALK and the subsequent translation of p80 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_provenance.
- NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_assertion evidence source_evidence_literature NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_provenance.
- NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_assertion SIO_000772 9561912 NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_provenance.
- NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_assertion wasDerivedFrom befree-20140225 NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_provenance.
- NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_assertion wasGeneratedBy ECO_0000203 NP408995.RALd4hBL7qAqSZdu6FV8zcvfvwLqnuGXgQitJ03lYj7fs130_provenance.