Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_assertion> ?p ?o ?g. }
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- NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_assertion type Assertion NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_head.
- NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_assertion description "[In addition, at a single nucleotide polymorphism upstream of PRNP thought to confer susceptibility to sporadic Creutzfeldt-Jakob disease (rs1029273), all patients were homozygous for the risk allele (combined P=5.9�10(-5)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_provenance.
- NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_assertion evidence source_evidence_literature NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_provenance.
- NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_assertion SIO_000772 21616973 NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_provenance.
- NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_assertion wasDerivedFrom befree-2016 NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_provenance.
- NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_assertion wasGeneratedBy ECO_0000203 NP897094.RAZ6CuG0pEO1S-3EscG6-o4k9gzc96IuIzZhA_EOanddA130_provenance.