Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_provenance.
- NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_assertion description "[A novel mutation in the HSD17B10 gene of a 10-year-old boy with refractory epilepsy, choreoathetosis and learning disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_provenance.
- NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_assertion evidence source_evidence_literature NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_provenance.
- NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_assertion SIO_000772 22132097 NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_provenance.
- NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_assertion wasDerivedFrom befree-20150227 NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_provenance.
- NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_assertion wasGeneratedBy ECO_0000203 NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP443145.RALyxi23JZuGSSTNJ3bkDJSRn08OPK68qRRiYOHgSniuc130_provenance.