Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP289365.RA4klHRIFjiJbuPraDZXE6ipWkpQaf3yn0gk5nPVAx1Ag130_provenance.