Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_provenance.
- NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_assertion description "[Polymorphisms of the ADR gene may alter the untreated IOP level of patients with NTG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_provenance.
- NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_assertion evidence source_evidence_literature NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_provenance.
- NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_assertion SIO_000772 20705341 NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_provenance.
- NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_assertion wasDerivedFrom gad-20150221 NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_provenance.
- NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_assertion wasGeneratedBy ECO_0000203 NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP183514.RAX0miOrNG3W7rH6x4N7oX-DnPWJohj7ClVVk5VxjcYAM130_provenance.