Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_assertion> ?p ?o ?g. }
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- NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_assertion type Assertion NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_head.
- NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_assertion description "[Neuroferritinopathies are dominantly inherited movement disorders associated with nucleotide insertions in the L-ferritin gene that modify the protein's C-terminus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_provenance.
- NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_assertion evidence source_evidence_literature NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_provenance.
- NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_assertion SIO_000772 19781644 NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_provenance.
- NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_assertion wasDerivedFrom befree-20140225 NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_provenance.
- NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_assertion wasGeneratedBy ECO_0000203 NP625617.RAP4NXV9ki2mjOoA8R-51NDb9njxFO1J_WA1mnLXEUd24130_provenance.