Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance.
- NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion description "[We studied the allelic frequencies of ApoE in 26 DS cases fulfilling clinical diagnostic criteria for AD and in 26 DS controls matched for age, sex, and premorbid level of mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance.
- NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion evidence source_evidence_literature NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance.
- NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion SIO_000772 7654070 NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance.
- NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion wasDerivedFrom befree-20140225 NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance.
- NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion wasGeneratedBy ECO_0000203 NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance.