Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_assertion> ?p ?o ?g. }
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- NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_assertion type Assertion NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_head.
- NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_provenance.
- NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_assertion evidence source_evidence_curated NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_provenance.
- NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_assertion SIO_000772 20817137 NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_provenance.
- NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_assertion wasDerivedFrom uniprot-20130724 NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_provenance.
- NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_assertion wasGeneratedBy ECO_0000218 NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_provenance.