Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_provenance.
- NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_assertion description "[We considered that the CHRD gene and the chordin-regulating GSC (goosecoid) gene could be candidate genes for Cornelia de Lange syndrome (CDLS), a developmental malformation syndrome which is primarily characterised by mental handicap, growth retardation, distinctive facial features and limb-reduction defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_provenance.
- NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_assertion evidence source_evidence_literature NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_provenance.
- NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_assertion SIO_000772 10480362 NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_provenance.
- NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_assertion wasDerivedFrom befree-2016 NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_provenance.
- NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_assertion wasGeneratedBy ECO_0000203 NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP262525.RAKPohGJfBCzO8f7ehWCYRFsCWQez6JoKEKwQxmfKyLFQ130_provenance.