Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_assertion> ?p ?o ?g. }
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- NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_assertion type Assertion NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_head.
- NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_assertion description "[Based on the large data collection of MLL genomic breakpoints in acute leukemias comprising more than 1.600 cases at the Diagnostic Center for Acute Leukemias (DCAL) in Frankfurt, Germany that provide an overview over the experimentally observed fusion transcript variants, we developed RT-PCR methods for the reliable detection of the 8 most common MLL aberrations (MLL-AF4, MLL-AF6, MLL-AF9, MLL-AF10, MLL-ENL, MLL-ELL, MLL-EPS15, MLL PTD), together accounting for around 90% of MLL-r cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_provenance.
- NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_assertion evidence source_evidence_literature NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_provenance.
- NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_assertion SIO_000772 25510485 NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_provenance.
- NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_assertion wasDerivedFrom befree-2016 NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_provenance.
- NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_assertion wasGeneratedBy ECO_0000203 NP1248215.RAPvpVkSsvi33LfGCuC19VHKmpMAqVvn0KFa_sLtBxFvo130_provenance.