Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP767584.RAQrrg8CWV7SS8Qep2DAkaTQmFDMFPYEiOcJLhOY2pkUI130_provenance.
- 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.