Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_assertion type Assertion NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_head.
- NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_assertion description "[These observations suggest that variations in PCSK9 are a rare cause of non LDLR/non APOB ADH (approximately 2.3%) and that additional environmental or genetic factors may contribute to the phenotype caused by PCSK9 missense mutations in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_provenance.
- NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_assertion evidence source_evidence_literature NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_provenance.
- NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_assertion SIO_000772 16211558 NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_provenance.
- NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_assertion wasDerivedFrom befree-2016 NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_provenance.
- NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_assertion wasGeneratedBy ECO_0000203 NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_provenance.