Matches in Nanopublications for { ?s ?p "[Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP359847.RAo6tsJwa8P7eyTbyPZpB4OvB1iQ5rASrqc39MKnXEsYI130_assertion description "[Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP359847.RAo6tsJwa8P7eyTbyPZpB4OvB1iQ5rASrqc39MKnXEsYI130_provenance.
- NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_assertion description "[Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_provenance.
- NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_assertion description "[Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539557.RAfLG16Er2EbYrvaqXfYfCkFSZB7KYSm6JOzcvDdEKDno130_provenance.
- assertion description "[Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1047799.RAezdIPeGNPpyZXlvp2afS394fhwp0uYwSuY9hpsNqYe8130_assertion description "[Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1047799.RAezdIPeGNPpyZXlvp2afS394fhwp0uYwSuY9hpsNqYe8130_provenance.
- NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_assertion description "[Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1047798.RAhT2zcOGh52MqID0BpvQ4p42oclJPOMkjlrF4rbJuWaU130_provenance.
- NP244406.RAHrauFlktEz70nAZto7CJdbdYFZtNc-dLmyAJWgumbJA130_assertion description "[Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP244406.RAHrauFlktEz70nAZto7CJdbdYFZtNc-dLmyAJWgumbJA130_provenance.