Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_provenance.
- NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_assertion description "[Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_provenance.
- NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_assertion evidence source_evidence_literature NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_provenance.
- NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_assertion SIO_000772 18723524 NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_provenance.
- NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_assertion wasDerivedFrom befree-2016 NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_provenance.
- NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_assertion wasGeneratedBy ECO_0000203 NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_provenance.
- befree-2016 importedOn "2016-02-19" NP689378.RA1_Qj0ty32V-DaUzaTdfXVRMe1kwsxwQxH6Bgrak2nC8130_provenance.