Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_provenance.
- NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_assertion description "[Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_provenance.
- NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_assertion evidence source_evidence_literature NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_provenance.
- NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_assertion SIO_000772 11090341 NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_provenance.
- NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_assertion wasDerivedFrom befree-20150227 NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_provenance.
- NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_assertion wasGeneratedBy ECO_0000203 NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936892.RAeddlhatGb2Ic7pUOBhI8zYUMIXaEwKt1k3P9e9byYKg130_provenance.