Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_assertion> ?p ?o ?g. }
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- NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_assertion type Assertion NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_head.
- NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_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." NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.
- NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_assertion evidence source_evidence_literature NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.
- NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_assertion SIO_000772 10480362 NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.
- NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_assertion wasDerivedFrom befree-20150227 NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.
- NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_assertion wasGeneratedBy ECO_0000203 NP974190.RAupT2bqvcXJ622KYjBxdIrCvh4aRZkW8r0BGw0L475VA130_provenance.