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- NP53698.RA99IWWjaMqius1xTCg5qPml38Z6D4QATRXBMEzNGABEM130_assertion type Assertion NP53698.RA99IWWjaMqius1xTCg5qPml38Z6D4QATRXBMEzNGABEM130_head.
- NP53698.RA99IWWjaMqius1xTCg5qPml38Z6D4QATRXBMEzNGABEM130_assertion wasGeneratedBy ECO_0000203 NP53698.RA99IWWjaMqius1xTCg5qPml38Z6D4QATRXBMEzNGABEM130_provenance.
- NP53698.RA99IWWjaMqius1xTCg5qPml38Z6D4QATRXBMEzNGABEM130_assertion wasDerivedFrom gad-20150221 NP53698.RA99IWWjaMqius1xTCg5qPml38Z6D4QATRXBMEzNGABEM130_provenance.
- NP53698.RA99IWWjaMqius1xTCg5qPml38Z6D4QATRXBMEzNGABEM130_assertion SIO_000772 11062157 NP53698.RA99IWWjaMqius1xTCg5qPml38Z6D4QATRXBMEzNGABEM130_provenance.
- NP53698.RA99IWWjaMqius1xTCg5qPml38Z6D4QATRXBMEzNGABEM130_assertion evidence source_evidence_literature NP53698.RA99IWWjaMqius1xTCg5qPml38Z6D4QATRXBMEzNGABEM130_provenance.
- NP53698.RA99IWWjaMqius1xTCg5qPml38Z6D4QATRXBMEzNGABEM130_assertion description "[Using this approach, possible associations of sequence variation, and hence of variation in DNA repair, with disease risk can be assessed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53698.RA99IWWjaMqius1xTCg5qPml38Z6D4QATRXBMEzNGABEM130_provenance.