Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_provenance.
- NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_assertion description "[The mutated alleles identified in our Japanese patients with OPMD were most likely due to duplications of (GCG)(3)GCA and (GCG)(2)(GCA)(3) but not simple expansions of the GCG repeats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_provenance.
- NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_assertion evidence source_evidence_literature NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_provenance.
- NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_assertion SIO_000772 11890856 NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_provenance.
- NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_assertion wasDerivedFrom befree-20140225 NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_provenance.
- NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_assertion wasGeneratedBy ECO_0000203 NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP609613.RA6movZZtqmnk8dGIrutf_b7GdSgyw_fZoTxfL23Ffnxk130_provenance.