Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_provenance.
- NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_provenance.
- NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_assertion evidence source_evidence_literature NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_provenance.
- NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_assertion SIO_000772 8744027 NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_provenance.
- NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_assertion wasDerivedFrom befree-2016 NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_provenance.
- NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_assertion wasGeneratedBy ECO_0000203 NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_provenance.