Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_assertion type Assertion NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_head.
- 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.
- NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_assertion evidence source_evidence_literature NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_provenance.
- NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_assertion SIO_000772 22155345 NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_provenance.
- NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_assertion wasDerivedFrom befree-20140225 NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_provenance.
- NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_assertion wasGeneratedBy ECO_0000203 NP235721.RAVyyMV5Nk2w-EZkkV-vpCUR-JRbeH2IoM3HrCTSCug9o130_provenance.