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- source_evidence_literature type ECO_0000212 NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP796163.RANHmglec7n0NAqhx8Cjc9ZLN0l0BXQAw_LeKZ4PFqC1I130_provenance.