Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_provenance.
- NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_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." NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_provenance.
- NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_assertion evidence source_evidence_literature NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_provenance.
- NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_assertion SIO_000772 22318346 NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_provenance.
- NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_assertion wasDerivedFrom befree-2016 NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_provenance.
- NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_assertion wasGeneratedBy ECO_0000203 NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_provenance.
- befree-2016 importedOn "2016-02-19" NP959507.RATOSqJYhlMkiebFdC4SUIS-iYZHRwZ4eL1odwmeniUWg130_provenance.