Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_provenance.
- NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_assertion description "[We investigated 12 cases of childhood ALL with TEL/AML1 gene fusion by fluorescence in situ hybridization (FISH) and comparative genomic hybridization (CGH) and documented additional or secondary genetic changes in seven patients (58%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_provenance.
- NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_assertion evidence source_evidence_literature NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_provenance.
- NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_assertion SIO_000772 11516105 NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_provenance.
- NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_assertion wasDerivedFrom befree-20140225 NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_provenance.
- NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_assertion wasGeneratedBy ECO_0000203 NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651149.RA_nFmnF7Da8OV4ROYX5ufV_X5_ZR5ichMlFuy64vz3KU130_provenance.