Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP955039.RAAItQ2qalMvLuv9SoC_BPD8YAQJkxk7VGH21jfSo0Uvw130_provenance.
- 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.