Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_provenance.
- NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_assertion description "[Mutations of FOXL2, a gene encoding a forkhead transcription factor, have been shown to cause the blepharophimosis-ptosis-epicanthus inversus syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_provenance.
- NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_assertion evidence source_evidence_literature NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_provenance.
- NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_assertion SIO_000772 16219626 NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_provenance.
- NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_assertion wasDerivedFrom befree-2016 NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_provenance.
- NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_assertion wasGeneratedBy ECO_0000203 NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_provenance.
- befree-2016 importedOn "2016-02-19" NP517585.RADd4d8wp2DxAnshGJ9eZDthJ8-5A-3q3Om2ihHxx9RIw130_provenance.