Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_provenance.
- NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_assertion description "[Here we describe another family with Snyder-Robinson syndrome in two Mexican brothers and a novel mutation (c.496T>G) in the exon 5 of the SMS gene confirming its involvement in this rare X-linked mental retardation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_provenance.
- NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_assertion evidence source_evidence_literature NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_provenance.
- NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_assertion SIO_000772 19206178 NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_provenance.
- NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_assertion wasDerivedFrom befree-20140225 NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_provenance.
- NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_assertion wasGeneratedBy ECO_0000203 NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP880980.RAARumjEEKlWoeWrIUoje0jQ8pm4Y_cKfHRwHxAqKLcjk130_provenance.