Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_provenance.
- NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_assertion wasGeneratedBy ECO_0000203 NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_provenance.
- NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_assertion wasDerivedFrom befree-20140225 NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_provenance.
- NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_assertion SIO_000772 1493642 NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_provenance.
- NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_assertion evidence source_evidence_literature NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_provenance.
- NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_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." NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP443735.RAWdR2buVDca1I93NesnD1-zUzdYbbjfcE2cOYpsOGnA0130_provenance.