Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_assertion type Assertion NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_head.
- NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_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." NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_provenance.
- NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_assertion evidence source_evidence_literature NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_provenance.
- NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_assertion SIO_000772 20042726 NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_provenance.
- NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_assertion wasDerivedFrom befree-2016 NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_provenance.
- NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_assertion wasGeneratedBy ECO_0000203 NP784368.RAm9cb0-kGkVJ9z_9TeHcO47lOy6lAsZZmf4UEzVlgxVM130_provenance.