Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_assertion type Assertion NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_head.
- NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_assertion description "[Parameter estimates from the ACE models of OAD and SAD showed that additive genetic variation was a necessary component in the explanation of individual differences in child-reported symptoms of OAD (h2 = .37) across gender, but does not appear to be a major contributor to the explanation of individual differences in symptoms of SAD reported by children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_provenance.
- NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_assertion evidence source_evidence_literature NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_provenance.
- NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_assertion SIO_000772 9145540 NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_provenance.
- NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_assertion wasDerivedFrom befree-20140225 NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_provenance.
- NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_assertion wasGeneratedBy ECO_0000203 NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_provenance.