Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_assertion description "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_provenance.
• NP889486.RAT9O30V_wruxAClW-QFH3kqNLt7byIyP7TXgs7dRRCyI130_assertion description "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889486.RAT9O30V_wruxAClW-QFH3kqNLt7byIyP7TXgs7dRRCyI130_provenance.
• NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_assertion description "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_provenance.
• NP717742.RA4gOAf2Xo6OqYR64U3I7DdQTh9GfEqeTbAjtaJJ81mS4130_assertion description "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717742.RA4gOAf2Xo6OqYR64U3I7DdQTh9GfEqeTbAjtaJJ81mS4130_provenance.
• NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_assertion description "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_provenance.
• NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_assertion description "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_provenance.
• assertion description "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP243869.RAt5SZrpBwTx_EYjy8mlTmSLOLbzrNJQFwOMUOfon58KI130_assertion description "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243869.RAt5SZrpBwTx_EYjy8mlTmSLOLbzrNJQFwOMUOfon58KI130_provenance.
• assertion description "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP945157.RAdcrIg7fy2avMjH064MO91GbpmC4E7w4tpG0ZDPaT8u8130_assertion description "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945157.RAdcrIg7fy2avMjH064MO91GbpmC4E7w4tpG0ZDPaT8u8130_provenance.
• NP894617.RAmKMu4uZEo61hIJMGTu5W4WStCgvTknOnUegjKUmhngc130_assertion description "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894617.RAmKMu4uZEo61hIJMGTu5W4WStCgvTknOnUegjKUmhngc130_provenance.
• NP945154.RA8gOC9hb9TPbHWLlESKwxiumqIwKWkUBz6MLqNbodSes130_assertion description "[The main genetic disorder associated with FHBL consists of mutations in the APOB gene, while other less frequent forms are associated with mutations in NPC1L1, PCSK9, a still unidentified gene in 3p21.1-22 and, more recently, in ANGPTL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945154.RA8gOC9hb9TPbHWLlESKwxiumqIwKWkUBz6MLqNbodSes130_provenance.