Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_assertion> ?p ?o ?g. }
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- NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_assertion type Assertion NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_head.
- NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_assertion wasGeneratedBy ECO_0000203 NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_provenance.
- NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_assertion wasDerivedFrom befree-20150227 NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_provenance.
- NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_assertion SIO_000772 22004887 NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_provenance.
- NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_assertion evidence source_evidence_literature NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_provenance.
- NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_assertion description "[Considering only the patients clearly diagnosed with Usher syndrome type II, and results obtained in this and previous studies, we can state that mutations in USH2A are responsible for 76.1% of USH2 disease in patients of Spanish origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_provenance.