Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_provenance.
- NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_assertion description "[The authors have identified a large Finnish kindred with presenile dementia and spastic paraparesis due to deletion of exon 9 of presenilin 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_provenance.
- NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_assertion evidence source_evidence_literature NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_provenance.
- NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_assertion SIO_000772 10720282 NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_provenance.
- NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_assertion wasDerivedFrom befree-2016 NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_provenance.
- NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_assertion wasGeneratedBy ECO_0000203 NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_provenance.
- befree-2016 importedOn "2016-02-19" NP278265.RAbh36kqMAphMNkUol6YrtyPedkdlCsoMyJj28Yp3f9Jg130_provenance.