Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_provenance.
- NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_assertion description "[Three VPS26A variants (p.K93E, p.M112V, and p.K297X), identified in patients with atypical parkinsonism, were not observed in controls from this study (n?=?368) or from publically available data sets (n?=?4,426).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_provenance.
- NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_assertion evidence source_evidence_literature NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_provenance.
- NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_assertion SIO_000772 25475142 NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_provenance.
- NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_assertion wasDerivedFrom befree-2016 NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_provenance.
- NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_assertion wasGeneratedBy ECO_0000203 NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244838.RA5QGkto0u_eflBt_SP3DvIaTIV6JvW9tdPqUaOE08QYk130_provenance.