Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_provenance.
- NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_assertion description "[Recent genome-wide association data have implicated genetic variation at 7p12.2 (IKZF1), 10q21.2 (ARIDB5), and 14q11.2 (CEBPE) in the etiology of B-cell childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_provenance.
- NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_assertion evidence source_evidence_literature NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_provenance.
- NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_assertion SIO_000772 20042726 NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_provenance.
- NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_assertion wasDerivedFrom gad-20130706 NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_provenance.
- NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_assertion wasGeneratedBy ECO_0000203 NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_provenance.
- gad-20130706 importedOn "2013-07-06" NP78070.RAlsX_y1i_eWBMsBfq3yBj26G78IsXSY4xapG8VVblS2s130_provenance.