Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_assertion> ?p ?o ?g. }
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- NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_assertion type Assertion NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_head.
- NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_provenance.
- NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_assertion evidence source_evidence_literature NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_provenance.
- NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_assertion SIO_000772 23941260 NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_provenance.
- NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_assertion wasDerivedFrom befree-20150227 NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_provenance.
- NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_assertion wasGeneratedBy ECO_0000203 NP227635.RA-YNWjeDzX8fCX4fxRPDOKcTaKEMos2DwyDmtmrsV6uw130_provenance.