Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP589811.RADZGOYwtXa5cHO0358Xc7K6A7ofQsak8FUlD9lNwU1P4130_provenance.