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- NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_assertion type Assertion NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_head.
- NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_assertion wasGeneratedBy ECO_0000203 NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_provenance.
- NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_assertion wasDerivedFrom lhgdn-20090331 NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_provenance.
- NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_assertion SIO_000772 15304595 NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_provenance.
- NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_assertion evidence source_evidence_literature NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_provenance.
- NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_assertion description "[a rare polymorphism at codon 171 (Asn-- > Ser) of human Prnp is associated with symptomatic epilepsies related to different forms of malformations of cortical development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP127024.RAWnYkhFDDeUxgYStW4gYXR1RzUpp6RONBainDONtNwnU130_provenance.