Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_provenance.
- NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_assertion description "[Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_provenance.
- NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_assertion evidence source_evidence_curated NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_provenance.
- NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_assertion SIO_000772 21460841 NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_provenance.
- NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_assertion wasDerivedFrom ctd_human-2016 NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_provenance.
- NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_assertion wasGeneratedBy ECO_0000218 NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP28907.RAdKYwmg7mrFUevc03X5Te7t3CMU18SRk7EHTzgYpeVSM130_provenance.