Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_assertion type Assertion NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_head.
- NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_assertion description "[Approximately 15% of cases of recognized prion disease are inherited and associated with coding mutations in the gene encoding prion protein (PRNP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_provenance.
- NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_assertion evidence source_evidence_literature NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_provenance.
- NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_assertion SIO_000772 24224623 NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_provenance.
- NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_assertion wasDerivedFrom befree-2016 NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_provenance.
- NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_assertion wasGeneratedBy ECO_0000203 NP1127702.RAvm_SjxsLVmER4PaSHdAMtX-O4CJOKQDkFWqFguusVoc130_provenance.