Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_provenance.
- NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_assertion wasGeneratedBy ECO_0000203 NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_provenance.
- NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_assertion wasDerivedFrom lhgdn-20090331 NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_provenance.
- NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_assertion SIO_000772 11857550 NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_provenance.
- NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_assertion evidence source_evidence_literature NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_provenance.
- NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_assertion description "[May be a modifier of a gene associated with Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP146566.RAmMn7t_o3_9I9IEYj_6Q8EjpHWiy6yOBl0TLpBPlDhj0130_provenance.