Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_provenance.
- NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_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." NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_provenance.
- NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_assertion evidence source_evidence_literature NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_provenance.
- NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_assertion SIO_000772 10480362 NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_provenance.
- NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_assertion wasDerivedFrom befree-20140225 NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_provenance.
- NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_assertion wasGeneratedBy ECO_0000203 NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP226240.RAQ6C-x1ezhqdDxEXBx2k3Kw_rv8sCoeEvulJyNBc3Luw130_provenance.