Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_assertion> ?p ?o ?g. }
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- NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_assertion type Assertion NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_head.
- NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_assertion wasGeneratedBy ECO_0000203 NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_provenance.
- NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_assertion wasDerivedFrom befree-20140225 NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_provenance.
- NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_assertion SIO_000772 7485229 NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_provenance.
- NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_assertion evidence source_evidence_literature NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_provenance.
- NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_assertion description "[Mutations in the amyloid protein are rare and segregate with the disease in a few early-onset familial AD (FAD) families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP170094.RAet_RyXdy0f57G8j34CcAYX4K1X_XSTDXLXCi0hIkqgI130_provenance.