Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_provenance.
- NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_assertion description "[The fragment was used to search for mutations of the corresponding gamma-cGMP-PDE gene in patients with autosomal dominant, autosomal recessive, or isolate case retinitis pigmentosa, and Usher's syndrome type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_provenance.
- NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_assertion evidence source_evidence_literature NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_provenance.
- NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_assertion SIO_000772 1683837 NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_provenance.
- NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_assertion wasDerivedFrom befree-20140225 NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_provenance.
- NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_assertion wasGeneratedBy ECO_0000203 NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212408.RADlj9Q8zVJa_gxGKP5W-ko-7_X-m2weedeGY1AXpHD0I130_provenance.