Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_assertion> ?p ?o ?g. }
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- NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_assertion type Assertion NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_head.
- NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_assertion description "[Smith-Lemli-Opitz syndrome (SLOS, RSH/SLO syndrome, MIM 270400) is an autosomal recessive multiple malformation/mental retardation syndrome initially described by Smith et al.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_provenance.
- NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_assertion evidence source_evidence_literature NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_provenance.
- NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_assertion SIO_000772 10899806 NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_provenance.
- NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_assertion wasDerivedFrom befree-2016 NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_provenance.
- NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_assertion wasGeneratedBy ECO_0000203 NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_provenance.