Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_provenance.
- NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_assertion description "[Genetic variability in the serotonin 2A (5-HT(2A)) receptor may influence risk for TD but the results of prior studies are not confirmatory.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_provenance.
- NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_assertion evidence source_evidence_literature NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_provenance.
- NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_assertion SIO_000772 15857569 NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_provenance.
- NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_assertion wasDerivedFrom befree-20140225 NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_provenance.
- NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_assertion wasGeneratedBy ECO_0000203 NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP727138.RAsAu4ocd8Dxu1EJNgx_vID31lUISttz-Qk2z7uyDvInU130_provenance.