Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_provenance.
- NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_assertion description "[A 3.5 y-old girl carrying a severe mutation of the LDL-receptor gene known as FH Pavia, affected by homozygous familial hypercholesterolaemia (FH), and at high risk of developing coronary artery atherosclerosis was treated with selective dextran sulphate cellulose (DSC) column low-density lipoprotein apheresis (LDL-a).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_provenance.
- NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_assertion evidence source_evidence_literature NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_provenance.
- NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_assertion SIO_000772 11440106 NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_provenance.
- NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_assertion wasDerivedFrom befree-2016 NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_provenance.
- NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_assertion wasGeneratedBy ECO_0000203 NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_provenance.
- befree-2016 importedOn "2016-02-19" NP322967.RAdISBEFXFD7TSJ4xza-jPvtGVFuzEk15h_koxywyD_ZM130_provenance.