Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_provenance.
- NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_assertion description "[This figure is comparable to the percentage of RP2 gene mutations that we have detected in our entire XLRP patient pool (10%-15%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_provenance.
- NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_assertion evidence source_evidence_literature NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_provenance.
- NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_assertion SIO_000772 10480356 NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_provenance.
- NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_assertion wasDerivedFrom befree-20140225 NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_provenance.
- NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_assertion wasGeneratedBy ECO_0000203 NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_provenance.