Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.
- NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_assertion description "[The authors identified a novel peripherin/RDS gene mutation associated with autosomal dominant retinal degeneration in patients from three different families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.
- NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_assertion evidence source_evidence_literature NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.
- NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_assertion SIO_000772 7862413 NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.
- NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_assertion wasDerivedFrom befree-20140225 NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.
- NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_assertion wasGeneratedBy ECO_0000203 NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP470973.RAfckxc08k6bm1HgBbAYBtzF8D_L26eGVsTI8pc3zbDV0130_provenance.