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- source_evidence_literature type ECO_0000212 NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_provenance.
- NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_assertion description "[In conclusion, we present compelling evidence for genetic heterogeneity within Europe. These NOD2/CARD15 variants have a minor contribution in Scottish and Irish CD patients, consistent with an emerging pattern from Northern Europe.Genes and Immunity adva]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_provenance.
- NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_assertion evidence source_evidence_literature NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_provenance.
- NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_assertion SIO_000772 15190267 NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_provenance.
- NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_assertion wasDerivedFrom gad-20150221 NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_provenance.
- NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_assertion wasGeneratedBy ECO_0000203 NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP57005.RACcdjn1pg_qxLNeVLcmRaR6pLvvTTiy9u49P9AZN_gEo130_provenance.