Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_provenance.
- NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_assertion description "[Functional impact of global rare copy number variation in autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_provenance.
- NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_assertion evidence source_evidence_curated NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_provenance.
- NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_assertion SIO_000772 20531469 NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_provenance.
- NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_assertion wasDerivedFrom ctd_human-20130708 NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_provenance.
- NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_assertion wasGeneratedBy ECO_0000218 NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_provenance.