Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_assertion> ?p ?o ?g. }
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- NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_assertion type Assertion NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_head.
- 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.
- NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_assertion evidence source_evidence_literature NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_provenance.
- NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_assertion SIO_000772 22155345 NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_provenance.
- NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_assertion wasDerivedFrom befree-20150227 NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_provenance.
- NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_assertion wasGeneratedBy ECO_0000203 NP894610.RAVRM9yLFU0nc98yAMhBMB0nXrhcn3ais92Vo3DHtNtxU130_provenance.