Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_assertion> ?p ?o ?g. }
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- NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_assertion type Assertion NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_head.
- NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_assertion description "[Minor allele homozygosity for this EL variant (c.584C>T) could be a significant risk factor for developing severe, sight-threatening disease due to proliferative DR. Further prospective studies of this EL polymorphism in a larger population sample are needed to confirm these results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_provenance.
- NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_assertion evidence source_evidence_literature NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_provenance.
- NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_assertion SIO_000772 24852509 NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_provenance.
- NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_assertion wasDerivedFrom befree-2016 NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_provenance.
- NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_assertion wasGeneratedBy ECO_0000203 NP1184640.RAcL0_mrtVF8kMwhLvea2WF0zGJlnhu2Fym0dVfh3PfUI130_provenance.