Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion description "[Subsequent studies demonstrated that this mutation is present in one-half of all CG1 patients and correlates with the Zellweger syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion evidence source_evidence_literature NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion SIO_000772 10447258 NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion wasDerivedFrom befree-20140225 NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion wasGeneratedBy ECO_0000203 NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.