Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_provenance.
- NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_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." NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_provenance.
- NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_assertion evidence source_evidence_literature NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_provenance.
- NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_assertion SIO_000772 11440106 NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_provenance.
- NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_assertion wasDerivedFrom befree-20140225 NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_provenance.
- NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_assertion wasGeneratedBy ECO_0000203 NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP914758.RA1RDXH5vMZz3iiOAepvWHXucKDLk9IWc_eXB0TvK9epo130_provenance.