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- source_evidence_literature type ECO_0000212 NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_provenance.
- NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_assertion description "[The findings support the association of several loci with AD, and suggest how intermediate phenotypes can enhance analysis of susceptibility loci in this complex genetic disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_provenance.
- NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_assertion evidence source_evidence_literature NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_provenance.
- NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_assertion SIO_000772 20574532 NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_provenance.
- NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_assertion wasDerivedFrom gad-20150221 NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_provenance.
- NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_assertion wasGeneratedBy ECO_0000203 NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP94972.RAk3Baer2_y7T6ILXOVYgwSfo6alki3jfwQKuspegJvPQ130_provenance.