Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_provenance.
- NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_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." NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_provenance.
- NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_assertion evidence source_evidence_literature NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_provenance.
- NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_assertion SIO_000772 15857569 NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_provenance.
- NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_assertion wasDerivedFrom befree-20150227 NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_provenance.
- NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_assertion wasGeneratedBy ECO_0000203 NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP471512.RAc5Xa9pYi_TNcmXioji2Ij6U63ciTWnGXvG4eskV30NA130_provenance.