Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_provenance.
- NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_assertion description "[In this work, we investigated for the first time, APOE and PRNP genotypes simultaneously in 474 AD and 175 sporadic CJD (sCJD) patients compared to a common control population of 335 subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_provenance.
- NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_assertion evidence source_evidence_literature NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_provenance.
- NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_assertion SIO_000772 21799773 NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_provenance.
- NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_assertion wasDerivedFrom befree-20140225 NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_provenance.
- NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_assertion wasGeneratedBy ECO_0000203 NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP378213.RAH1zPLBd6Bh9TPdjfaDRTiZPmuzc-n3FqPaKUuJQrgxA130_provenance.