Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_provenance.
- NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_assertion description "[The multifactorial genetic dysfunction in AD includes mutational loci (APP, PS1, PS2) and diverse susceptibility loci (APOE, A2M, AACT, LRP1, IL1A, TNF, ACE, BACE, BCHE, CST3, MTHFR, GSK3B, NOS3) distributed across the human genome, probably converging in common pathogenic mechanisms that lead to premature neuronal death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_provenance.
- NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_assertion evidence source_evidence_literature NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_provenance.
- NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_assertion SIO_000772 12452480 NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_provenance.
- NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_assertion wasDerivedFrom befree-20140225 NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_provenance.
- NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_assertion wasGeneratedBy ECO_0000203 NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP269766.RAJIyOIkNdBLPkoVFlT6Y5VA9pVrlYIPah_ZfcyhHw3n4130_provenance.