Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_assertion> ?p ?o ?g. }
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- NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_assertion type Assertion NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_head.
- NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_assertion wasGeneratedBy ECO_0000203 NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_provenance.
- NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_assertion wasDerivedFrom befree-20140225 NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_provenance.
- NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_assertion SIO_000772 23144630 NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_provenance.
- NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_assertion evidence source_evidence_literature NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_provenance.
- NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_assertion description "[Heterozygous mutations in the PRPF31 gene cause autosomal dominant retinitis pigmentosa (adRP), a hereditary disorder leading to progressive blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218471.RAzUH7vrJx9YNkr8SIjj7RBrvyZN-aPoyZw13uVYOosuo130_provenance.