Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_assertion> ?p ?o ?g. }
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- NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_assertion type Assertion NP13880.RA2oVErAHop6iS_XEMnXLxvftKGllvPMixZAsZAI0vbsM130_head.
- 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.