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- source_evidence_literature type ECO_0000212 NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_provenance.
- NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_assertion description "[Large de novo deletion of 7p15.1 to 7p12.1 involving the imprinted gene GRB10 associated with a complex phenotype including features of Beckwith Wiedemann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_provenance.
- NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_assertion evidence source_evidence_literature NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_provenance.
- NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_assertion SIO_000772 20933618 NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_provenance.
- NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_assertion wasDerivedFrom befree-20150227 NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_provenance.
- NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_assertion wasGeneratedBy ECO_0000203 NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP433660.RAr5IHh-wf68tfsOpRn-jmGWSUaQYlXhyZwb-BbMrHh_c130_provenance.