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- NP199727.RADUFYcUGvywbUJKJbo8ebYEIcCofWYyIDrk997owyAeg130_assertion type Assertion NP199727.RADUFYcUGvywbUJKJbo8ebYEIcCofWYyIDrk997owyAeg130_head.
- NP199727.RADUFYcUGvywbUJKJbo8ebYEIcCofWYyIDrk997owyAeg130_assertion wasGeneratedBy ECO_0000203 NP199727.RADUFYcUGvywbUJKJbo8ebYEIcCofWYyIDrk997owyAeg130_provenance.
- NP199727.RADUFYcUGvywbUJKJbo8ebYEIcCofWYyIDrk997owyAeg130_assertion wasDerivedFrom befree-20140225 NP199727.RADUFYcUGvywbUJKJbo8ebYEIcCofWYyIDrk997owyAeg130_provenance.
- NP199727.RADUFYcUGvywbUJKJbo8ebYEIcCofWYyIDrk997owyAeg130_assertion SIO_000772 11803489 NP199727.RADUFYcUGvywbUJKJbo8ebYEIcCofWYyIDrk997owyAeg130_provenance.
- NP199727.RADUFYcUGvywbUJKJbo8ebYEIcCofWYyIDrk997owyAeg130_assertion evidence source_evidence_literature NP199727.RADUFYcUGvywbUJKJbo8ebYEIcCofWYyIDrk997owyAeg130_provenance.
- NP199727.RADUFYcUGvywbUJKJbo8ebYEIcCofWYyIDrk997owyAeg130_assertion description "[No statistically significant association was observed between sequence variants in the ELOVL(4) gene and susceptibility to AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199727.RADUFYcUGvywbUJKJbo8ebYEIcCofWYyIDrk997owyAeg130_provenance.