Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_provenance.
- NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_assertion description "[Genetic polymorphisms in the 3'UTR region of the CXCL12 (rs1801157) and TP53 codon 72 (rs1042522) genes may contribute to susceptibility to childhood ALL because they affect some important processes, such as metastasis regulation and tumor suppression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_provenance.
- NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_assertion evidence source_evidence_literature NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_provenance.
- NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_assertion SIO_000772 23653000 NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_provenance.
- NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_assertion wasDerivedFrom befree-20140225 NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_provenance.
- NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_assertion wasGeneratedBy ECO_0000203 NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP581174.RAdt01EKyWQJ4R00DKfrdvY1n922YtpMLaDUWVNYUKykM130_provenance.