Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_assertion> ?p ?o ?g. }
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- NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_assertion type Assertion NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_head.
- NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_assertion wasGeneratedBy ECO_0000203 NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_provenance.
- NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_assertion wasDerivedFrom befree-20150227 NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_provenance.
- NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_assertion SIO_000772 22076464 NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_provenance.
- NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_assertion evidence source_evidence_literature NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_provenance.
- NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_assertion description "[We performed a genome-wide association study of 355 750 single-nucleotide polymorphisms (SNPs) in 474 controls and 419 childhood ALL cases characterized by a t(12;21)(p13;q22) - the most common chromosomal translocation observed in childhood ALL - which leads to an ETV6-RUNX1 gene fusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387105.RA4g_i3OYcwZ3KJBjq3AxX9_ZuijhsXyf26jwFYa92jy4130_provenance.