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- source_evidence_literature type ECO_0000212 NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_provenance.
- NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_assertion description "[Markers rs4151659 (mapping to CFB) and rs7762619 (mapping 5' of LTA) were the most strongly associated with T1D on DR3 (P=1.2 x 10(-9) and P=2 x 10(-12), respectively) and DR4 (P=4 x 10(-15) and P=8 x 10(-8), respectively) haplotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_provenance.
- NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_assertion evidence source_evidence_literature NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_provenance.
- NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_assertion SIO_000772 20054343 NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_provenance.
- NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_assertion wasDerivedFrom befree-2016 NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_provenance.
- NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_assertion wasGeneratedBy ECO_0000203 NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_provenance.
- befree-2016 importedOn "2016-02-19" NP785413.RAv54OvwnZp3vnDGQSfvipmOj_W__S3gANMcWCRJedeWc130_provenance.