Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_provenance.
- NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_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." NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_provenance.
- NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_assertion evidence source_evidence_literature NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_provenance.
- NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_assertion SIO_000772 24369382 NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_provenance.
- NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_assertion wasDerivedFrom befree-20150227 NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_provenance.
- NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_assertion wasGeneratedBy ECO_0000203 NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP759012.RA-w4BKoGfbP7-0cVta75v52cD9kiwOYkpt8QL7T7S_HQ130_provenance.