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- source_evidence_literature type ECO_0000212 NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_provenance.
- NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_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." NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_provenance.
- NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_assertion evidence source_evidence_literature NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_provenance.
- NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_assertion SIO_000772 25625642 NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_provenance.
- NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_assertion wasDerivedFrom befree-2016 NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_provenance.
- NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_assertion wasGeneratedBy ECO_0000203 NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1258820.RA2-_EXJi51pYOHcgmrfEzo71tzhlMzw6YmhgWjuONsZA130_provenance.