Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_assertion type Assertion NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_head.
- NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_provenance.
- NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_assertion evidence source_evidence_literature NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_provenance.
- NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_assertion SIO_000772 17273969 NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_provenance.
- NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_assertion wasDerivedFrom befree-20150227 NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_provenance.
- NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_assertion wasGeneratedBy ECO_0000203 NP976671.RAJHITfUyJ5iJfmLGAFaoMKvbCPhM8O2ro8EK5iFca4w4130_provenance.