Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_provenance.
- NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_assertion description "[Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_provenance.
- NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_assertion evidence source_evidence_literature NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_provenance.
- NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_assertion SIO_000772 20140240 NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_provenance.
- NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_assertion wasDerivedFrom befree-20140225 NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_provenance.
- NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_assertion wasGeneratedBy ECO_0000203 NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP739135.RAT3MhLOgXeDlzrI-TVvBMVumOailOdvnP5jF27dgFlQ0130_provenance.