Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_assertion type Assertion NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_head.
- NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_assertion description "[To estimate the prevalence of CESD in different populations, the frequencies of the c.894G>A mutation were determined in 10,000 LIPA alleles from healthy African-American, Asian, Caucasian, Hispanic, and Ashkenazi Jewish individuals from the greater New York metropolitan area and 6,578 LIPA alleles from African-American, Caucasian, and Hispanic subjects enrolled in the Dallas Heart Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_provenance.
- NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_assertion evidence source_evidence_literature NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_provenance.
- NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_assertion SIO_000772 23424026 NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_provenance.
- NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_assertion wasDerivedFrom befree-20140225 NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_provenance.
- NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_assertion wasGeneratedBy ECO_0000203 NP464128.RA5rNCBRQgt_qPys29de5hzQ-SmO6gM_PVVhw9UooHRJU130_provenance.