Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_assertion> ?p ?o ?g. }
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- NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_assertion type Assertion NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_head.
- NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_assertion description "[In humans, we identified recessive loss-of-function DYX1C1 mutations in 12 individuals with PCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_provenance.
- NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_assertion evidence source_evidence_literature NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_provenance.
- NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_assertion SIO_000772 23872636 NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_provenance.
- NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_assertion wasDerivedFrom befree-2016 NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_provenance.
- NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_assertion wasGeneratedBy ECO_0000203 NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_provenance.