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- NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_assertion type Assertion NP579279.RAlhTT-m6elGTtnwcvQC_G_CwG3rHfJ5TqcGatuPXLgmU130_head.
- 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.