Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_provenance.
- NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_assertion description "[Here we report a frequency of 11.2% of mutations and variants in the known Alzheimer disease genes in the dementia cohort studied and 24% in the early onset subgroup of patients, suggesting that mutations in these genes are not uncommon in Turkey and are associated with various phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_provenance.
- NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_assertion evidence source_evidence_literature NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_provenance.
- NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_assertion SIO_000772 22503161 NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_provenance.
- NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_assertion wasDerivedFrom befree-2016 NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_provenance.
- NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_assertion wasGeneratedBy ECO_0000203 NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_provenance.
- befree-2016 importedOn "2016-02-19" NP974761.RAfJFXWtQHhbNaYIkjr2a7kBfOSC1QTwZdqMnhG0sTEec130_provenance.