Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_provenance.
- NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_assertion description "[The combination of the T variant of the 1858 polymorphism of the PTPN22 gene in combination with the presence of anti-CCP antibodies, preferentially in a SE-positive individual, is associated with the development of RA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_provenance.
- NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_assertion evidence source_evidence_literature NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_provenance.
- NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_assertion SIO_000772 18156150 NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_provenance.
- NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_assertion wasDerivedFrom befree-2016 NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_provenance.
- NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_assertion wasGeneratedBy ECO_0000203 NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_provenance.
- befree-2016 importedOn "2016-02-19" NP646819.RAj9i4kvuU1d9FsyEX4Hp8RL9pF91qfC-3eWIWNLBEOy0130_provenance.