Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.
- befree-2016 importedOn "2016-02-19" NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.
- NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_assertion wasGeneratedBy ECO_0000203 NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.
- NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_assertion wasDerivedFrom befree-2016 NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.
- NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_assertion SIO_000772 21799773 NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.
- NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_assertion evidence source_evidence_literature NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_provenance.
- NP913263.RAk2AJ5G7Enab8PVYQT5zTuBYzzEL313dHb1XMn2E1e44130_assertion description "[It is well-established that the APOE ε4 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.