Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_provenance.
- NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_assertion description "[The HDR syndrome has been described in patients with mutations affecting both ZnF1 and ZnF2 domains; the former result in inefficient interaction with FOG, and the latter result in disruption of DNA binding.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_provenance.
- NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_assertion evidence source_evidence_literature NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_provenance.
- NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_assertion SIO_000772 15705923 NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_provenance.
- NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_assertion wasDerivedFrom befree-20140225 NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_provenance.
- NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_assertion wasGeneratedBy ECO_0000203 NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP410553.RAu-nCbz2CZ8ZBf1BpWdqmWzBZErobBKtrid_55dgsSSk130_provenance.