Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_provenance.
- NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_assertion description "[Familial lecithin cholesterol acyltransferase (LCAT) deficiency is a rare inherited enzyme deficiency characterized by widespread disturbance of lipid metabolism and infiltration of many organs, including kidneys by lipids; usually it results in death from renal failure in the fourth or fifth decades.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_provenance.
- NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_assertion evidence source_evidence_literature NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_provenance.
- NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_assertion SIO_000772 7156322 NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_provenance.
- NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_assertion wasDerivedFrom befree-2016 NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_provenance.
- NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_assertion wasGeneratedBy ECO_0000203 NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_provenance.