Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_provenance.
- NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_assertion description "[In this longitudinal study of adolescents with 22q11.2 deletion syndrome, we identified the catechol-O-methyltransferase low-activity allele (COMT(L)) as a risk factor for decline in prefrontal cortical volume and cognition, as well as for the consequent development of psychotic symptoms during adolescence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_provenance.
- NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_assertion evidence source_evidence_literature NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_provenance.
- NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_assertion SIO_000772 16234808 NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_provenance.
- NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_assertion wasDerivedFrom befree-20150227 NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_provenance.
- NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_assertion wasGeneratedBy ECO_0000203 NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_provenance.
- befree-20150227 importedOn "2015-02-27" NP322144.RAFS-tin_HBjEd3xXCF8ke84NiWRt44uSxwpHs2Q4Vh20130_provenance.