Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_assertion type Assertion NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_head.
- NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_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." NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_provenance.
- NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_assertion evidence source_evidence_literature NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_provenance.
- NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_assertion SIO_000772 25625642 NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_provenance.
- NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_assertion wasDerivedFrom befree-2016 NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_provenance.
- NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_assertion wasGeneratedBy ECO_0000203 NP1258824.RAENUy-_FvKaU14DhvDhKtwrPJ7rfGvUFqIYyVO8qceEI130_provenance.