Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_assertion> ?p ?o ?g. }
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- NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_assertion type Assertion NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_head.
- NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_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." NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_provenance.
- NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_assertion evidence source_evidence_literature NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_provenance.
- NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_assertion SIO_000772 1679288 NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_provenance.
- NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_assertion wasDerivedFrom befree-2016 NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_provenance.
- NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_assertion wasGeneratedBy ECO_0000203 NP556113.RAVR-PgUcRTJB2PI8HMv4ETx7kdr1n8RshYdfqKhC7xm0130_provenance.