Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_provenance.
- NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_assertion description "[These SNPs are in or near genes that are highly expressed in the brain (HECW2, HIP1, BIN2, GRIA1), genes involved in neural development and function (KCNQ4, LMO4, GRIA1, NETO1) and autophagy (ATG4C), and genes that are associated with risk of various diseases including cancer and Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_provenance.
- NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_assertion evidence source_evidence_literature NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_provenance.
- NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_assertion SIO_000772 21782286 NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_provenance.
- NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_assertion wasDerivedFrom befree-20140225 NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_provenance.
- NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_assertion wasGeneratedBy ECO_0000203 NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP339122.RAJatVSOvPKPHn2iFPe6oarIaBxWe5JpDsQS0RDrIgk1I130_provenance.