Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_provenance.
- NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_assertion description "[Evidence is presented suggesting that apoprotein-E2 homozygosity in our patient, together with an 88% reduction in plasma lipoprotein lipase activity associated with severe nephrotic syndrome, is responsible for the atypical clinical features, lipoprotein phenotype III with chylomicronemia, and renal lipidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_provenance.
- NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_assertion evidence source_evidence_literature NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_provenance.
- NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_assertion SIO_000772 8589283 NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_provenance.
- NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_assertion wasDerivedFrom befree-20150227 NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_provenance.
- NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_assertion wasGeneratedBy ECO_0000203 NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP539359.RA8sRe_B1XA0PSnHbOf6nsLNml5VtzzJrRm93RBvhVqfc130_provenance.