Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_provenance.
- NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_assertion description "[A mutation in the 3'-UTR of the HDAC6 gene abolishing the post-transcriptional regulation mediated by hsa-miR-433 is linked to a new form of dominant X-linked chondrodysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_provenance.
- NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_assertion evidence source_evidence_literature NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_provenance.
- NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_assertion SIO_000772 20181727 NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_provenance.
- NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_assertion wasDerivedFrom befree-20140225 NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_provenance.
- NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_assertion wasGeneratedBy ECO_0000203 NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP898681.RAB3R6SlZZBBtZbGxr9KJYyv213IwpfOA7k9z1jFHgdXA130_provenance.