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- NP52809.RAPR6Z215KVMG7O5l0ftNO2_EQEtFinSxZHymADeyVLdg130_assertion type Assertion NP52809.RAPR6Z215KVMG7O5l0ftNO2_EQEtFinSxZHymADeyVLdg130_head.
- NP52809.RAPR6Z215KVMG7O5l0ftNO2_EQEtFinSxZHymADeyVLdg130_assertion wasGeneratedBy ECO_0000203 NP52809.RAPR6Z215KVMG7O5l0ftNO2_EQEtFinSxZHymADeyVLdg130_provenance.
- NP52809.RAPR6Z215KVMG7O5l0ftNO2_EQEtFinSxZHymADeyVLdg130_assertion wasDerivedFrom gad-20130706 NP52809.RAPR6Z215KVMG7O5l0ftNO2_EQEtFinSxZHymADeyVLdg130_provenance.
- NP52809.RAPR6Z215KVMG7O5l0ftNO2_EQEtFinSxZHymADeyVLdg130_assertion SIO_000772 16298355 NP52809.RAPR6Z215KVMG7O5l0ftNO2_EQEtFinSxZHymADeyVLdg130_provenance.
- NP52809.RAPR6Z215KVMG7O5l0ftNO2_EQEtFinSxZHymADeyVLdg130_assertion evidence source_evidence_literature NP52809.RAPR6Z215KVMG7O5l0ftNO2_EQEtFinSxZHymADeyVLdg130_provenance.
- NP52809.RAPR6Z215KVMG7O5l0ftNO2_EQEtFinSxZHymADeyVLdg130_assertion description "[ While any single mutation causes only a mildly increased LR (none > 1.7), in combination, the likelihood of early-onset CAD increased to 2.78 with four mutations. The genetics of early-onset CAD appear to be multifactorial, requiring polygenic models to elucidate risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52809.RAPR6Z215KVMG7O5l0ftNO2_EQEtFinSxZHymADeyVLdg130_provenance.