Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_provenance.
- befree-2016 importedOn "2016-02-19" NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_provenance.
- NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_assertion wasGeneratedBy ECO_0000203 NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_provenance.
- NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_assertion wasDerivedFrom befree-2016 NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_provenance.
- NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_assertion SIO_000772 21204217 NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_provenance.
- NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_assertion evidence source_evidence_literature NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_provenance.
- NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_assertion description "[Although we could not identify any nucleotide alteration in DYRK1A and KCNJ6 in our cohort study for 150 patients with mental retardation with/without epilepsy, this study underscores the clinical importance of DSCR not only for DS but also for developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862860.RAT9T75MepQCWP7UUB0BhIg-rGANMUm3EbWhTbE6AUsWE130_provenance.