Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_provenance.
- NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_assertion description "[In initial and validation analyses, SLX4IP deletions were significantly associated with male gender and ETV6/RUNX1-rearranged ALL (both overall P < 0.0001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_provenance.
- NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_assertion evidence source_evidence_literature NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_provenance.
- NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_assertion SIO_000772 24045615 NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_provenance.
- NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_assertion wasDerivedFrom befree-2016 NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_provenance.
- NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_assertion wasGeneratedBy ECO_0000203 NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1111684.RA4e9K0HB7fQA4EZ6URvw2IOKjCTNH3av7TtjCRFTsPRs130_provenance.