Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_assertion> ?p ?o ?g. }
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- NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_assertion type Assertion NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_head.
- NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_assertion wasGeneratedBy ECO_0000203 NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_provenance.
- NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_assertion wasDerivedFrom gad-20150221 NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_provenance.
- NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_assertion SIO_000772 20531469 NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_provenance.
- NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_assertion evidence source_evidence_literature NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_provenance.
- NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_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." NP177898.RA3ljuwGzozlIn5vN4sCGZf3YbWR2Lq39H0Jm47Z5UUnE130_provenance.