Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_assertion> ?p ?o ?g. }
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- NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_assertion type Assertion NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_head.
- NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_assertion description "[The PRNP variant allele Asn171Ser is associated with epileptogenesis and highly prevalent in patients with medically untreatable mesial temporal sclerosis with hippocampal sclerosis and influences their surgical outcome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_provenance.
- NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_assertion evidence source_evidence_literature NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_provenance.
- NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_assertion SIO_000772 14610121 NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_provenance.
- NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_assertion wasDerivedFrom lhgdn-20090331 NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_provenance.
- NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_assertion wasGeneratedBy ECO_0000203 NP133500.RAC5TlrC0-dukz6Hr1W37coUmFZsqMWw5y4l8Jfhc3cnU130_provenance.