Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_provenance.
- NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_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." NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_provenance.
- NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_assertion evidence source_evidence_literature NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_provenance.
- NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_assertion SIO_000772 20042726 NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_provenance.
- NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_assertion wasDerivedFrom befree-20150227 NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_provenance.
- NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_assertion wasGeneratedBy ECO_0000203 NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_provenance.
- befree-20150227 importedOn "2015-02-27" NP840652.RAWbAxyyx1Wt7-gECRueN5VCUB8K1NjaVgUT7uiknUn64130_provenance.