Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_assertion> ?p ?o ?g. }
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- NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_assertion type Assertion NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_head.
- NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_assertion description "[Data presented here does not support the role of common genetic variation in OXTR in the aetiology of autism spectrum disorders in Caucasian samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_provenance.
- NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_assertion evidence source_evidence_literature NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_provenance.
- NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_assertion SIO_000772 20303388 NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_provenance.
- NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_assertion wasDerivedFrom befree-20140225 NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_provenance.
- NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_assertion wasGeneratedBy ECO_0000203 NP620586.RA1nIdzmfHheppBJ_sC7L5s9mjXnsZg8oglre_6iu0g58130_provenance.