Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_provenance.
- NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_assertion description "[To clarify the prevalence of SCA15 in Japan, we designed four sets of probes and primers in different regions of ITPR1 and performed TaqMan PCR assay to search for gene deletions in 226 index SCA patients excluded for repeat expansion disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_provenance.
- NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_assertion evidence source_evidence_literature NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_provenance.
- NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_assertion SIO_000772 22318346 NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_provenance.
- NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_assertion wasDerivedFrom befree-20150227 NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_provenance.
- NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_assertion wasGeneratedBy ECO_0000203 NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP518755.RAvezC4ZImdClgVo8Ex0ngYGGIoGOFlkkYNqV4UqwNaBo130_provenance.