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- NP745473.RAySULn-Euen41kVB_D9caKgHdjNr45L_Dtafm2ZS7a3s130_assertion type Assertion NP745473.RAySULn-Euen41kVB_D9caKgHdjNr45L_Dtafm2ZS7a3s130_head.
- NP745473.RAySULn-Euen41kVB_D9caKgHdjNr45L_Dtafm2ZS7a3s130_assertion wasGeneratedBy ECO_0000203 NP745473.RAySULn-Euen41kVB_D9caKgHdjNr45L_Dtafm2ZS7a3s130_provenance.
- NP745473.RAySULn-Euen41kVB_D9caKgHdjNr45L_Dtafm2ZS7a3s130_assertion wasDerivedFrom befree-20140225 NP745473.RAySULn-Euen41kVB_D9caKgHdjNr45L_Dtafm2ZS7a3s130_provenance.
- NP745473.RAySULn-Euen41kVB_D9caKgHdjNr45L_Dtafm2ZS7a3s130_assertion SIO_000772 17272748 NP745473.RAySULn-Euen41kVB_D9caKgHdjNr45L_Dtafm2ZS7a3s130_provenance.
- NP745473.RAySULn-Euen41kVB_D9caKgHdjNr45L_Dtafm2ZS7a3s130_assertion evidence source_evidence_literature NP745473.RAySULn-Euen41kVB_D9caKgHdjNr45L_Dtafm2ZS7a3s130_provenance.
- NP745473.RAySULn-Euen41kVB_D9caKgHdjNr45L_Dtafm2ZS7a3s130_assertion description "[High frequency of a retinoid X receptor gamma gene variant in familial combined hyperlipidemia that associates with atherogenic dyslipidemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745473.RAySULn-Euen41kVB_D9caKgHdjNr45L_Dtafm2ZS7a3s130_provenance.