Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_provenance.
- NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_assertion wasGeneratedBy ECO_0000203 NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_provenance.
- NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_assertion wasDerivedFrom befree-20140225 NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_provenance.
- NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_assertion SIO_000772 1493642 NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_provenance.
- NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_assertion evidence source_evidence_literature NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_provenance.
- NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_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." NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_provenance.