Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_provenance.
- NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_assertion description "[Two genes, Semaphorin F (SEMAF) and delta-catenin (CTNND2), which have been mapped to the `critical regions`, are potentially involved in cerebral development and their deletion may be associated with mental retardation in CdCS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_provenance.
- NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_assertion evidence source_evidence_literature NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_provenance.
- NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_assertion SIO_000772 16953888 NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_provenance.
- NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_assertion wasDerivedFrom befree-20140225 NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_provenance.
- NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_assertion wasGeneratedBy ECO_0000203 NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP906520.RA63K47e5OxX-8Yspk1xMMGGePeiOPXKi0JxE2u8GPAK0130_provenance.