Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_assertion type Assertion NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_head.
- NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_assertion description "[In the present study, we analysed the PCSK9 coding region and intronic junctions in 130 adult or pediatric patients with ADH, previously found as being non LDLR/non APOB mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_provenance.
- NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_assertion evidence source_evidence_literature NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_provenance.
- NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_assertion SIO_000772 16211558 NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_provenance.
- NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_assertion wasDerivedFrom befree-20140225 NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_provenance.
- NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_assertion wasGeneratedBy ECO_0000203 NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_provenance.