Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_provenance.
- NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_assertion description "[Recently, the functional defect of ADRA2A has been implicated as a cause of depression, attention deficit hyperactivity disorder, and Tourette syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_provenance.
- NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_assertion evidence source_evidence_literature NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_provenance.
- NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_assertion SIO_000772 18794646 NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_provenance.
- NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_assertion wasDerivedFrom befree-20140225 NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_provenance.
- NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_assertion wasGeneratedBy ECO_0000203 NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP601371.RAXY9gV4M8NoCInfNGGyRmYETmvLspK8BTOCNNmOAomXE130_provenance.