Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_provenance.
- NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_assertion description "[No significant differences in genotypes frequencies of the CYP2D6 C100T polymorphism were observed between patients with TD and without TD (Chi2=4.078, P>0.05), but patients with TD had a significant excess of the T allele compared with those without TD (Chi2=4.28, P<0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_provenance.
- NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_assertion evidence source_evidence_literature NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_provenance.
- NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_assertion SIO_000772 16490169 NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_provenance.
- NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_assertion wasDerivedFrom befree-20140225 NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_provenance.
- NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_assertion wasGeneratedBy ECO_0000203 NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP625483.RA3oVRVx9ZKqly2PuJxCY5e-3JygToxu3kjlZTo_1huj4130_provenance.