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- NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_assertion type Assertion NP223229.RA7_ATQMFT3eIVjlkyI4MK4423bYH8rjPB45SVrW7gb9k130_head.
- 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.