Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_provenance.
- NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_assertion description "[Mutations in lipoprotein lipase (LPL), apolipoprotein CII (APOC2), lipase maturation factor 1 (LMF1), glycosyl-phosphatidylinositol anchored high-density lipoprotein-binding protein 1 (GPIHBP1), and apolipoprotein AV (APOA5) cause T1HLP, but we lack data on phenotypic variations among the different genetic subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_provenance.
- NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_assertion evidence source_evidence_literature NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_provenance.
- NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_assertion SIO_000772 24793350 NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_provenance.
- NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_assertion wasDerivedFrom befree-2016 NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_provenance.
- NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_assertion wasGeneratedBy ECO_0000203 NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_provenance.
- befree-2016 importedOn "2016-02-19" NP1179103.RAz9uzTsBvK4DX5HYpYiozxToRk4FKabYFiS5cgdLDT4I130_provenance.