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- NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_assertion type Assertion NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_head.
- NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_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." NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_provenance.
- NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_assertion evidence source_evidence_literature NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_provenance.
- NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_assertion SIO_000772 19781644 NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_provenance.
- NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_assertion wasDerivedFrom befree-20140225 NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_provenance.
- NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_assertion wasGeneratedBy ECO_0000203 NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_provenance.