Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_provenance.
- NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_assertion wasGeneratedBy ECO_0000203 NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_provenance.
- NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_assertion wasDerivedFrom befree-20140225 NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_provenance.
- NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_assertion SIO_000772 12783988 NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_provenance.
- NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_assertion evidence source_evidence_literature NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_provenance.
- NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_assertion description "[The lipodystrophy mutation R482Q, which causes a different phenotype and is believed to act through an emerin-independent mechanism, was indistinguishable from wild-type in its localization and its ability to trap emerin at the nuclear rim.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP759603.RAZOc5xJiiy5SNhfiWca315_DN5wIgXPvvOT44rf31RjU130_provenance.