Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_provenance.
- NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_assertion description "[The objective of this clinical-pathologic study was to identify biomarkers for a pallidopontonigral degeneration (PPND) kindred of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) harboring the N279K tau mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_provenance.
- NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_assertion evidence source_evidence_literature NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_provenance.
- NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_assertion SIO_000772 17196872 NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_provenance.
- NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_assertion wasDerivedFrom befree-2016 NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_provenance.
- NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_assertion wasGeneratedBy ECO_0000203 NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_provenance.
- befree-2016 importedOn "2016-02-19" NP586647.RAt7EfeouTi-Lkf0UFta7pzsS3LYJGMfNV1a54rDd0goo130_provenance.