Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_provenance.
- NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_assertion wasGeneratedBy ECO_0000203 NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_provenance.
- NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_assertion wasDerivedFrom befree-20150227 NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_provenance.
- NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_assertion SIO_000772 24870754 NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_provenance.
- NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_assertion evidence source_evidence_literature NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_provenance.
- NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_assertion description "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284933.RAOsvTEIXEfIW1yzsy3YRacqWPOoJKytVUf1OEr1hHVS4130_provenance.