Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_provenance.
- NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_assertion description "[Microdeletions of movement disorder genes including epsilon-sarcoglycan (SGCE) and thyroid transcription factor-1 (TITF1) have been described in patients with myoclonus dystonia and benign hereditary chorea respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_provenance.
- NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_assertion evidence source_evidence_literature NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_provenance.
- NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_assertion SIO_000772 22515636 NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_provenance.
- NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_assertion wasDerivedFrom befree-20140225 NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_provenance.
- NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_assertion wasGeneratedBy ECO_0000203 NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP883893.RA96Jvzs4khN1clRQxPmA4ZD_Oij0Ncqu-4YOdDRMVYjE130_provenance.