Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_provenance.
- NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_assertion description "[The authors previously reported that genetic variation in the gene coding for nicastrin (NCSTN) modified risk for familial early-onset Alzheimer disease (AD) in a Dutch population-based sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_provenance.
- NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_assertion evidence source_evidence_literature NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_provenance.
- NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_assertion SIO_000772 15249634 NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_provenance.
- NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_assertion wasDerivedFrom befree-20140225 NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_provenance.
- NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_assertion wasGeneratedBy ECO_0000203 NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP293315.RAlosXGaw3mFLW5CcUcNF66cfpn6_tmrLRXbgV1EILX9A130_provenance.