Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_provenance.
- NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_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." NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_provenance.
- NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_assertion evidence source_evidence_literature NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_provenance.
- NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_assertion SIO_000772 22155345 NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_provenance.
- NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_assertion wasDerivedFrom befree-20140225 NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_provenance.
- NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_assertion wasGeneratedBy ECO_0000203 NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP863764.RAddvPUttMWg-xmLQhj-ZMoe7WPr7jR46aQNgypxQqfoY130_provenance.