Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_provenance.
- NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_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." NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_provenance.
- NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_assertion evidence source_evidence_literature NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_provenance.
- NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_assertion SIO_000772 9145540 NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_provenance.
- NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_assertion wasDerivedFrom befree-2016 NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_provenance.
- NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_assertion wasGeneratedBy ECO_0000203 NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1372554.RARRlBK6PJ3Ea8iQS0uifI8NsGrU4mxB9h7JghRvmAdc0130_provenance.