Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_provenance.
- NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_assertion description "[Identification and characterization of human NR4A2 polymorphisms in attention deficit hyperactivity disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_provenance.
- NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_assertion evidence source_evidence_literature NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_provenance.
- NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_assertion SIO_000772 15635701 NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_provenance.
- NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_assertion wasDerivedFrom befree-20140225 NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_provenance.
- NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_assertion wasGeneratedBy ECO_0000203 NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP702099.RAr7jmf63ENDLNc1EfCYcxY_cuKkYK4NG_swVJcKeIlC4130_provenance.