Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_assertion> ?p ?o ?g. }
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- NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_assertion type Assertion NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_head.
- NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_assertion description "[Here we describe a unique case of childhood NMZL with unusual clinicopathologic features for the pediatric variant including generalized lymphadenopathy, high-stage disease with persistence after therapy, unusual immunophenotype (CD5, CD23, and BCL6 positive), and unique chromosomal abnormalities including monosomy 20 and add(10)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_provenance.
- NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_assertion evidence source_evidence_literature NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_provenance.
- NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_assertion SIO_000772 25625642 NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_provenance.
- NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_assertion wasDerivedFrom befree-2016 NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_provenance.
- NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_assertion wasGeneratedBy ECO_0000203 NP1258821.RAcAhGk3pgfWLWdHSjkF0wMBM39AnMP4kp6XoOht0kvA4130_provenance.