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- NP661015.RAhswPuHMqL_GMM8GYzBxnML_ZPLRoHu_mLNrRL0j_vrs130_assertion type Assertion NP661015.RAhswPuHMqL_GMM8GYzBxnML_ZPLRoHu_mLNrRL0j_vrs130_head.
- NP661015.RAhswPuHMqL_GMM8GYzBxnML_ZPLRoHu_mLNrRL0j_vrs130_assertion description "[In conclusion, LRP gene polymorphisms, particularly the relatively common exon 22 C200T polymorphism, are a significant risk factor for premature CAD in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661015.RAhswPuHMqL_GMM8GYzBxnML_ZPLRoHu_mLNrRL0j_vrs130_provenance.
- NP661015.RAhswPuHMqL_GMM8GYzBxnML_ZPLRoHu_mLNrRL0j_vrs130_assertion evidence source_evidence_literature NP661015.RAhswPuHMqL_GMM8GYzBxnML_ZPLRoHu_mLNrRL0j_vrs130_provenance.
- NP661015.RAhswPuHMqL_GMM8GYzBxnML_ZPLRoHu_mLNrRL0j_vrs130_assertion SIO_000772 12732394 NP661015.RAhswPuHMqL_GMM8GYzBxnML_ZPLRoHu_mLNrRL0j_vrs130_provenance.
- NP661015.RAhswPuHMqL_GMM8GYzBxnML_ZPLRoHu_mLNrRL0j_vrs130_assertion wasDerivedFrom befree-20150227 NP661015.RAhswPuHMqL_GMM8GYzBxnML_ZPLRoHu_mLNrRL0j_vrs130_provenance.
- NP661015.RAhswPuHMqL_GMM8GYzBxnML_ZPLRoHu_mLNrRL0j_vrs130_assertion wasGeneratedBy ECO_0000203 NP661015.RAhswPuHMqL_GMM8GYzBxnML_ZPLRoHu_mLNrRL0j_vrs130_provenance.