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- source_evidence_literature type ECO_0000212 NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_provenance.
- NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_assertion description "[Here, we describe the detection of cryptic or variant PML-RARA rearrangements by translocation-based comparative genomic hybridization (tCGH), a recently described modification of traditional CGH technology that facilitates the detection of balanced translocations by means of the linear amplification of a potential translocation breakpoint region(s), in 2 unusual cases of APL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_provenance.
- NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_assertion evidence source_evidence_literature NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_provenance.
- NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_assertion SIO_000772 23370423 NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_provenance.
- NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_assertion wasDerivedFrom befree-20150227 NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_provenance.
- NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_assertion wasGeneratedBy ECO_0000203 NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP470289.RAd_08HwG1QWVm91R7-YPTi2UvU89tNPGO51tSvdh46p8130_provenance.