Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_provenance.
- NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_assertion description "[In the 22q11.2 deletion syndrome group, baseline subthreshold psychotic symptoms interacted both with the COMT genotype and with baseline symptoms of anxiety or depression to predict 61% of the variance in severity of psychosis at follow-up evaluation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_provenance.
- NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_assertion evidence source_evidence_literature NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_provenance.
- NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_assertion SIO_000772 17403981 NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_provenance.
- NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_assertion wasDerivedFrom befree-20140225 NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_provenance.
- NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_assertion wasGeneratedBy ECO_0000203 NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP155594.RAJ63j0U8VFdekXSmVvFC2Wx3mPEfxB9KHuOYyg_npGlQ130_provenance.