Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_provenance.
- NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_assertion description "[A pronounced lack of Frataxin causes Friedreich's Ataxia, which is a human neurodegenerative and hereditary disease mainly affecting the equilibrium, coordination, muscles and heart.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_provenance.
- NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_assertion evidence source_evidence_literature NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_provenance.
- NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_assertion SIO_000772 23463383 NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_provenance.
- NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_assertion wasDerivedFrom befree-20150227 NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_provenance.
- NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_assertion wasGeneratedBy ECO_0000203 NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP411409.RAcSizIahWo3T6vWOljwwkzTapK3RMoHLZ1msVacUM44M130_provenance.