Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_provenance.
- NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_assertion description "[A molecular case report of autosomal dominant retinitis pigmentosa: RP1/RHO sequence variants in a Turkish family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_provenance.
- NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_assertion evidence source_evidence_literature NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_provenance.
- NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_assertion SIO_000772 22321012 NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_provenance.
- NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_assertion wasDerivedFrom befree-2016 NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_provenance.
- NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_assertion wasGeneratedBy ECO_0000203 NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_provenance.
- befree-2016 importedOn "2016-02-19" NP959725.RApVGlW8LLZND43Dg1CTGSbUZ7sR8ms2wUma5uVGAs24c130_provenance.