Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_assertion> ?p ?o ?g. }
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- NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_assertion type Assertion NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_head.
- 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.
- NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_assertion evidence source_evidence_literature NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_provenance.
- NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_assertion SIO_000772 22155345 NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_provenance.
- NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_assertion wasDerivedFrom befree-20140225 NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_provenance.
- NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_assertion wasGeneratedBy ECO_0000203 NP616889.RAPwldj2CeUdihq6KvmDrkYIceZ6wI7UjIJeeaUktfLpY130_provenance.