Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_provenance.
- NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_assertion description "[The DRB1*01 allele was expressed with a frequency of 20.69% in the controls whereas it was only detected in 3.96% of the NPC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_provenance.
- NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_assertion evidence source_evidence_literature NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_provenance.
- NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_assertion SIO_000772 19714482 NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_provenance.
- NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_assertion wasDerivedFrom befree-20150227 NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_provenance.
- NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_assertion wasGeneratedBy ECO_0000203 NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP456201.RAvVLOgBB7ZttfGEJwt-2CZXw_luuasJ5oHYEN8mWfJUY130_provenance.