Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_provenance.
- NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_assertion description "[COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_provenance.
- NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_assertion evidence source_evidence_literature NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_provenance.
- NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_assertion SIO_000772 16234808 NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_provenance.
- NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_assertion wasDerivedFrom befree-2016 NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_provenance.
- NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_assertion wasGeneratedBy ECO_0000203 NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_provenance.
- befree-2016 importedOn "2016-02-19" NP518611.RAnJqtYS3e73TNq-kRK0N8CymoXkzOzStEBDp4qKP1Vvw130_provenance.