Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_provenance.
- NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_assertion description "[Recent genome-wide association data have implicated genetic variation at 7p12.2 (IKZF1), 10q21.2 (ARIDB5), and 14q11.2 (CEBPE) in the etiology of B-cell childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_provenance.
- NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_assertion evidence source_evidence_literature NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_provenance.
- NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_assertion SIO_000772 20042726 NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_provenance.
- NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_assertion wasDerivedFrom befree-20140225 NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_provenance.
- NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_assertion wasGeneratedBy ECO_0000203 NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP616090.RAZMO9LAVEw7imV0nfWqpWqotG3wMgfwD5tIh5znhoQsk130_provenance.