Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_provenance.
- NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_assertion description "[Four SNPs across the PRF1 gene locus, 5 for GZMB, 7 for UNC13D, and 11 for Rab27a were investigated using MassArray genotyping in 133 UK Caucasian patients with systemic-onset JIA and 384 ethnically matched unrelated control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_provenance.
- NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_assertion evidence source_evidence_literature NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_provenance.
- NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_assertion SIO_000772 18311812 NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_provenance.
- NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_assertion wasDerivedFrom gad-20150221 NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_provenance.
- NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_assertion wasGeneratedBy ECO_0000203 NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP144883.RAMfXtRPIFH16Jz8pYiz9oLIW5R3V59Ij30fP93OW8zhQ130_provenance.