Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.
- befree-2016 importedOn "2016-02-19" NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.
- NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_assertion wasGeneratedBy ECO_0000203 NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.
- NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_assertion wasDerivedFrom befree-2016 NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.
- NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_assertion SIO_000772 16550584 NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.
- NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_assertion evidence source_evidence_literature NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.
- NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_assertion description "[Missense mutations in CDH23 have been associated with presbycusis and DFNB12, whereas null alleles cause the majority of Usher 1D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.