Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP394918.RAkWisCazAshpHd1ysr9OeTVgogbre6Wrul0xB1HaAbbs130_provenance.