Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP517079.RA_YjQ6xVkIHvwieIIYCR6k5xGPNBjMcIW__CG3tM3DEc130_provenance.