Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_provenance.
- NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_assertion wasGeneratedBy ECO_0000203 NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_provenance.
- NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_assertion wasDerivedFrom befree-20140225 NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_provenance.
- NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_assertion SIO_000772 20186779 NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_provenance.
- NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_assertion evidence source_evidence_literature NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_provenance.
- NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_assertion description "[In one Iranian family segregating autosomal recessive non-syndromic hearing loss (ARNSHL), we identified a homozygous variant in a predicted miR-96/182 binding site in the 3'UTR of the RDX (DFNB24) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP631876.RAXgaJhv0pf8eAjYr9XTLcs0jxVIOixFnpCClbwKprcGk130_provenance.