Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_provenance.
- NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_assertion wasGeneratedBy ECO_0000203 NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_provenance.
- NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_assertion wasDerivedFrom befree-20150227 NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_provenance.
- NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_assertion SIO_000772 23335487 NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_provenance.
- NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_assertion evidence source_evidence_literature NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_provenance.
- NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_assertion description "[Our data reveal a broad range of epimutations exist in certain imprinting syndromes, with the exception of Prader-Willi syndrome and Angelman syndrome patients that are associated with solitary SNRPN-DMR defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961025.RArgS9jY_N7tJsBD96EsLvJ6tZ0Cuto2MM6i_Yno8Bboc130_provenance.