Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_provenance.
- NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_assertion description "[Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_provenance.
- NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_assertion evidence source_evidence_literature NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_provenance.
- NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_assertion SIO_000772 22318346 NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_provenance.
- NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_assertion wasDerivedFrom befree-2016 NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_provenance.
- NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_assertion wasGeneratedBy ECO_0000203 NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_provenance.
- befree-2016 importedOn "2016-02-19" NP959509.RAwT56djZIOUkbVcM5Dx3uMdlEYQftrAoI5OHocX-O2iE130_provenance.