Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_assertion> ?p ?o ?g. }
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- NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_assertion type Assertion NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_head.
- NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_assertion description "[This includes cell lines derived from patients with relapsed disease featuring cytogenetic anomalies such as t(12;21), Philadelphia chromosome t(9;22), t(1;19) as well as a cell line carrying t(17;19) from a patient with de novo ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_provenance.
- NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_assertion evidence source_evidence_literature NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_provenance.
- NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_assertion SIO_000772 21960246 NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_provenance.
- NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_assertion wasDerivedFrom befree-20140225 NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_provenance.
- NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_assertion wasGeneratedBy ECO_0000203 NP376560.RAI81xpLyFCnN6QtQYZVU-1I1xzj6BJfwAUWfbRjTS8cs130_provenance.