Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_provenance.
- befree-2016 importedOn "2016-02-19" NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_provenance.
- NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_assertion wasGeneratedBy ECO_0000203 NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_provenance.
- NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_assertion wasDerivedFrom befree-2016 NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_provenance.
- NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_assertion SIO_000772 1493642 NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_provenance.
- NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_assertion evidence source_evidence_literature NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_provenance.
- NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_assertion description "[This receptor-binding defective apolipoprotein B variant is the cause of familial defective apo B-100 (FDB), an autosomal dominantly inherited disease, which leads to increased plasma cholesterol levels and premature atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431476.RADT44NKwFCMA-oI9DdsmQLFqwTartwd9re2haD9tikVs130_provenance.