Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_provenance.
- NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_assertion description "[We concluded that the NOS1 3'-UTR C276T polymorphism might not play a major role in the susceptibility of TD development, or on the severity of TD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_provenance.
- NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_assertion evidence source_evidence_literature NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_provenance.
- NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_assertion SIO_000772 15088155 NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_provenance.
- NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_assertion wasDerivedFrom befree-2016 NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_provenance.
- NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_assertion wasGeneratedBy ECO_0000203 NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_provenance.
- befree-2016 importedOn "2016-02-19" NP440287.RAiIre-8-dzLFubrI_mNVU3Ljg8nt8-T-1cUuvFhAelqY130_provenance.