Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_provenance.
- NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_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." NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_provenance.
- NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_assertion evidence source_evidence_literature NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_provenance.
- NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_assertion SIO_000772 10686945 NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_provenance.
- NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_assertion wasDerivedFrom befree-20140225 NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_provenance.
- NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_assertion wasGeneratedBy ECO_0000203 NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_provenance.
- befree-20140225 importedOn "2014-02-25" NP820608.RADcl-yBHa0FClXKot1a_T5WMQfYTfYUl-jp6lSp1Sj40130_provenance.