Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_provenance.
- NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_assertion description "[Tardive dyskinesia is not associated with the polymorphisms of 5-HT2A receptor gene, serotonin transporter gene and catechol-o-methyltransferase gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_provenance.
- NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_assertion evidence source_evidence_literature NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_provenance.
- NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_assertion SIO_000772 12711403 NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_provenance.
- NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_assertion wasDerivedFrom befree-20140225 NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_provenance.
- NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_assertion wasGeneratedBy ECO_0000203 NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP266407.RAFKmFzwRohXbRGMQAmJCr6YEmtdae-Ir7WVU93-w1FSU130_provenance.