Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_provenance.
- NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_assertion description "[We focused on the overlapping symptoms between CFS and MDD and performed an association study of the functional single-nucleotide polymorphism (SNP) in the DISC1 gene with CFS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_provenance.
- NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_assertion evidence source_evidence_literature NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_provenance.
- NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_assertion SIO_000772 20227423 NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_provenance.
- NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_assertion wasDerivedFrom befree-2016 NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_provenance.
- NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_assertion wasGeneratedBy ECO_0000203 NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_provenance.
- befree-2016 importedOn "2016-02-19" NP799688.RA5i3mwZXfEdhrtxAtdDltP3ap5qiG0BnIotJStBkZFyg130_provenance.