Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_provenance.
- NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_assertion wasGeneratedBy ECO_0000203 NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_provenance.
- NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_assertion wasDerivedFrom befree-20150227 NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_provenance.
- NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_assertion SIO_000772 21930553 NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_provenance.
- NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_assertion evidence source_evidence_literature NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_provenance.
- NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_assertion description "[A child with mild X-linked intellectual disability and a microduplication at Xp22.12 including RPS6KA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675638.RA3nkOTfwxaqBrDv-2EZBIMccdE3qd7qg_22HTdwOWsUc130_provenance.