Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.
- NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_assertion description "[Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.
- NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_assertion evidence source_evidence_literature NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.
- NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_assertion SIO_000772 19623215 NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.
- NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_assertion wasDerivedFrom befree-20150227 NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.
- NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_assertion wasGeneratedBy ECO_0000203 NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP404355.RAyq12q4MVxTfprTWjB6Q8FYW6tuMtceMQb9y_KYb9ngY130_provenance.