Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_provenance.
- NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_assertion description "[36 (82%) of the patients with BCR-ABL1-like disease had deletions in genes involved in B-cell development, including IKZF1, TCF3, EBF1, PAX5, and VPREB1; only nine (36%) of 25 patients with B-other ALL had deletions in these genes (p=0.0002).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_provenance.
- NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_assertion evidence source_evidence_literature NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_provenance.
- NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_assertion SIO_000772 19138562 NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_provenance.
- NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_assertion wasDerivedFrom befree-20140225 NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_provenance.
- NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_assertion wasGeneratedBy ECO_0000203 NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP756183.RAx-lKq-Qtql58HF6_oiK0KyFpyM8ul4GG2GTMphFQrl8130_provenance.