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- NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_assertion type Assertion NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_head.
- NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_assertion wasGeneratedBy ECO_0000203 NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_provenance.
- NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_assertion wasDerivedFrom befree-20150227 NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_provenance.
- NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_assertion SIO_000772 23322642 NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_provenance.
- NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_assertion evidence source_evidence_literature NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_provenance.
- NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_assertion description "[Striking intrafamilial phenotypic variability in Aicardi-Goutières syndrome associated with the recurrent Asian founder mutation in RNASEH2C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_provenance.