Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.
- NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_assertion description "[Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at least three genetic subtypes (USH2A, USH2B, and USH2C) and is classified phenotypically as congenital hearing loss and progressive retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.
- NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_assertion evidence source_evidence_literature NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.
- NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_assertion SIO_000772 14740321 NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.
- NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_assertion wasDerivedFrom befree-20140225 NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.
- NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_assertion wasGeneratedBy ECO_0000203 NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP740024.RAxh3ZhiLTqRJwqCTACpIOmanuC9uOy1eE9L8vWmqK1hw130_provenance.