Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_assertion> ?p ?o ?g. }
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- NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_assertion type Assertion NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_head.
- NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_assertion description "[It is well-established that the APOE ?4 allele and homozygosity at polymorphic codon 129 in the PRNP gene are the major genetic risk factors for AD and human prion diseases, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.
- NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_assertion evidence source_evidence_literature NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.
- NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_assertion SIO_000772 21799773 NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.
- NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_assertion wasDerivedFrom befree-2016 NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.
- NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_assertion wasGeneratedBy ECO_0000203 NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.