Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_provenance.
- NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_assertion description "[APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_provenance.
- NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_assertion evidence source_evidence_literature NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_provenance.
- NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_assertion SIO_000772 1679288 NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_provenance.
- NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_assertion wasDerivedFrom befree-20140225 NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_provenance.
- NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_assertion wasGeneratedBy ECO_0000203 NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP404257.RAlSUyPyaVQOguTtKS54e1Ze2OsDRrU4heH9Ct7hPFtwo130_provenance.