Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_assertion> ?p ?o ?g. }
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- NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_assertion type Assertion NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_head.
- NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_assertion description "[We describe the establishment and characterization of a new neuroblastoma (Nb) cell line, SiMa, carrying the major recurrent chromosome changes associated with poor prognosis Nb, including amplification of N-MYC by formation of double minutes (dmin), der(1)t(1;17)(p35;q12) and der(22)t(17;22)(q22;p13), and loss of chromosome 11, documented at both initiation and late passage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_provenance.
- NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_assertion evidence source_evidence_literature NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_provenance.
- NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_assertion SIO_000772 10686945 NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_provenance.
- NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_assertion wasDerivedFrom befree-20140225 NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_provenance.
- NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_assertion wasGeneratedBy ECO_0000203 NP909869.RAqeaoXSgYcCHrLZlqTlI7Otw4IAOtQyc7fRDIi0pzUwM130_provenance.