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- source_evidence_literature type ECO_0000212 NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_provenance.
- befree-2016 importedOn "2016-02-19" NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_provenance.
- NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_assertion wasGeneratedBy ECO_0000203 NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_provenance.
- NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_assertion wasDerivedFrom befree-2016 NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_provenance.
- NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_assertion SIO_000772 22076464 NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_provenance.
- NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_assertion evidence source_evidence_literature NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_provenance.
- NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_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." NP938123.RA9o8ObIDSGcMvlNX8GHwi8UoPBf4Hf-9TzHUeqmPa9B0130_provenance.