Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_provenance.
- befree-20150227 importedOn "2015-02-27" NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_provenance.
- NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_assertion wasGeneratedBy ECO_0000203 NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_provenance.
- NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_assertion wasDerivedFrom befree-20150227 NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_provenance.
- NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_assertion SIO_000772 22076464 NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_provenance.
- NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_assertion evidence source_evidence_literature NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_provenance.
- NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_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." NP289210.RA3qjS4kDaRGcrBsD-Dpb1rcatC8EBfsrJYvZd0Zw08ns130_provenance.