Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_provenance.
- NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_assertion description "[Our data suggest that the PTPN22 C1858T single nucleotide polymorphism has no or minor effect on RA and AITDs susceptibility in the Tunisian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_provenance.
- NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_assertion evidence source_evidence_literature NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_provenance.
- NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_assertion SIO_000772 19343596 NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_provenance.
- NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_assertion wasDerivedFrom befree-2016 NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_provenance.
- NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_assertion wasGeneratedBy ECO_0000203 NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_provenance.
- befree-2016 importedOn "2016-02-19" NP730382.RARVh3nVLfrFA0GshBrC5GT29oMmEW-eqr220tyieYKOM130_provenance.