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- NP1216496.RA0wWFXpS0WIK2Koik8oNDSje_T3Df8eYlpGEsy-5rLpI130_assertion type Assertion NP1216496.RA0wWFXpS0WIK2Koik8oNDSje_T3Df8eYlpGEsy-5rLpI130_head.
- NP1216496.RA0wWFXpS0WIK2Koik8oNDSje_T3Df8eYlpGEsy-5rLpI130_assertion description "[Early findings suggested that rare and low-frequency coding variation might have a large effect on human phenotypes (eg, PCSK9 missense variants on low-density lipoprotein-cholesterol and coronary heart diseases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216496.RA0wWFXpS0WIK2Koik8oNDSje_T3Df8eYlpGEsy-5rLpI130_provenance.
- NP1216496.RA0wWFXpS0WIK2Koik8oNDSje_T3Df8eYlpGEsy-5rLpI130_assertion evidence source_evidence_literature NP1216496.RA0wWFXpS0WIK2Koik8oNDSje_T3Df8eYlpGEsy-5rLpI130_provenance.
- NP1216496.RA0wWFXpS0WIK2Koik8oNDSje_T3Df8eYlpGEsy-5rLpI130_assertion SIO_000772 25185437 NP1216496.RA0wWFXpS0WIK2Koik8oNDSje_T3Df8eYlpGEsy-5rLpI130_provenance.
- NP1216496.RA0wWFXpS0WIK2Koik8oNDSje_T3Df8eYlpGEsy-5rLpI130_assertion wasDerivedFrom befree-2016 NP1216496.RA0wWFXpS0WIK2Koik8oNDSje_T3Df8eYlpGEsy-5rLpI130_provenance.
- NP1216496.RA0wWFXpS0WIK2Koik8oNDSje_T3Df8eYlpGEsy-5rLpI130_assertion wasGeneratedBy ECO_0000203 NP1216496.RA0wWFXpS0WIK2Koik8oNDSje_T3Df8eYlpGEsy-5rLpI130_provenance.