Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_provenance.
- NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_assertion description "[Her son's axial length was shortened with refractive errors of +16.75 dioptres in the right and +14.0 dioptres in the left eye; ERG evidenced a rod-cone dystrophy, OCT showed central macular thickening with cystoid changes and ultrasonography revealed optic disc drusen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_provenance.
- NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_assertion evidence source_evidence_literature NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_provenance.
- NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_assertion SIO_000772 23143909 NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_provenance.
- NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_assertion wasDerivedFrom befree-20140225 NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_provenance.
- NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_assertion wasGeneratedBy ECO_0000203 NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP883785.RARbhhjylN4mCzkAJAHDWQMe5FBmJYx5FxAnTrDEJsq-U130_provenance.