Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_provenance.
- NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_assertion description "[These new models, termed APP(NL-F) and APP(NL-G-F), have endogenous APP levels and develop robust A? amyloidosis, which induce synaptic degeneration and memory impairments.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_provenance.
- NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_assertion evidence source_evidence_literature NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_provenance.
- NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_assertion SIO_000772 24852598 NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_provenance.
- NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_assertion wasDerivedFrom befree-2016 NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_provenance.
- NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_assertion wasGeneratedBy ECO_0000203 NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1184649.RAHsD7FpQpKWPq6Mp8lD6fGHfUgIwPwDHrTMHtCGTE2gA130_provenance.