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- NP938121.RAQxY2bduV4HMqJmUq1_srAMPh4bvwM8-C5OwcK8zpxxw130_assertion type Assertion NP938121.RAQxY2bduV4HMqJmUq1_srAMPh4bvwM8-C5OwcK8zpxxw130_head.
- NP938121.RAQxY2bduV4HMqJmUq1_srAMPh4bvwM8-C5OwcK8zpxxw130_assertion wasGeneratedBy ECO_0000203 NP938121.RAQxY2bduV4HMqJmUq1_srAMPh4bvwM8-C5OwcK8zpxxw130_provenance.
- NP938121.RAQxY2bduV4HMqJmUq1_srAMPh4bvwM8-C5OwcK8zpxxw130_assertion wasDerivedFrom befree-2016 NP938121.RAQxY2bduV4HMqJmUq1_srAMPh4bvwM8-C5OwcK8zpxxw130_provenance.
- NP938121.RAQxY2bduV4HMqJmUq1_srAMPh4bvwM8-C5OwcK8zpxxw130_assertion SIO_000772 22076464 NP938121.RAQxY2bduV4HMqJmUq1_srAMPh4bvwM8-C5OwcK8zpxxw130_provenance.
- NP938121.RAQxY2bduV4HMqJmUq1_srAMPh4bvwM8-C5OwcK8zpxxw130_assertion evidence source_evidence_literature NP938121.RAQxY2bduV4HMqJmUq1_srAMPh4bvwM8-C5OwcK8zpxxw130_provenance.
- NP938121.RAQxY2bduV4HMqJmUq1_srAMPh4bvwM8-C5OwcK8zpxxw130_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." NP938121.RAQxY2bduV4HMqJmUq1_srAMPh4bvwM8-C5OwcK8zpxxw130_provenance.