Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.
- NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_assertion description "[We focus on a newly described human immunodeficiency disorder called radiosensitivity, immunodeficiency dysmorphic features and learning difficulties (RIDDLE) syndrome, with particular reference to the function of the defective gene, RNF168.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.
- NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_assertion evidence source_evidence_literature NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.
- NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_assertion SIO_000772 21426255 NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.
- NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_assertion wasDerivedFrom befree-2016 NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.
- NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_assertion wasGeneratedBy ECO_0000203 NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.
- befree-2016 importedOn "2016-02-19" NP881457.RAtQcZqhsAbiFF2vhAZCbyto7vZqri0B81rSYjRmOIAEY130_provenance.