Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_provenance.
- NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_assertion description "[The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_provenance.
- NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_assertion evidence source_evidence_curated NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_provenance.
- NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_assertion SIO_000772 24369382 NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_provenance.
- NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_assertion wasDerivedFrom uniprot-20150221 NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_provenance.
- NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_assertion wasGeneratedBy ECO_0000218 NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP4897.RAcSGHk-cA133Fe9Ch0iPL4l6Jq1Mni03j9WEedEx3AtI130_provenance.