Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_assertion> ?p ?o ?g. }
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- NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_assertion type Assertion NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_head.
- NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_assertion description "[These data show that mutations in ABC1 are the major cause of familial HDL deficiency associated with defective cholesterol efflux, and that CERP has an essential role in the formation of HDL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_provenance.
- NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_assertion evidence source_evidence_literature NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_provenance.
- NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_assertion SIO_000772 10533863 NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_provenance.
- NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_assertion wasDerivedFrom befree-20140225 NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_provenance.
- NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_assertion wasGeneratedBy ECO_0000203 NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_provenance.