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- source_evidence_literature type ECO_0000212 NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_provenance.
- NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_assertion description "[Selected candidate genes mapping within the aberrant genomic regions were sequenced and mutation of the TP53 gene was observed in one case in BC and of the ASXL1 gene in 6 of 41 cases in CP or BC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_provenance.
- NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_assertion evidence source_evidence_literature NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_provenance.
- NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_assertion SIO_000772 20410925 NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_provenance.
- NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_assertion wasDerivedFrom befree-20150227 NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_provenance.
- NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_assertion wasGeneratedBy ECO_0000203 NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978415.RA3WS0T3WkQxHwnD9qxbZFW4zaoFDjmjk2A-BzF8EO2ZM130_provenance.