Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_assertion> ?p ?o ?g. }
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- NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_assertion type Assertion NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_head.
- NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_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." NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_provenance.
- NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_assertion evidence source_evidence_literature NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_provenance.
- NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_assertion SIO_000772 10480362 NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_provenance.
- NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_assertion wasDerivedFrom befree-20140225 NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_provenance.
- NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_assertion wasGeneratedBy ECO_0000203 NP915419.RAfK9NvaxGPuF0DbrQ-dTLqHyAyO8mOo2j65foxZcKQmU130_provenance.