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- source_evidence_literature type ECO_0000212 NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_provenance.
- NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_assertion description "[Genetic variation in a region on chromosome 11 that contains the candidate genes AMBRA1, DGKZ, CHRM4 and MDK was significantly associated with SCZ in the combined sample (n=11?540; P=3.89 � 10(-9), odds ratio (OR)=1.25).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_provenance.
- NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_assertion evidence source_evidence_literature NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_provenance.
- NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_assertion SIO_000772 21747397 NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_provenance.
- NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_assertion wasDerivedFrom befree-2016 NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_provenance.
- NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_assertion wasGeneratedBy ECO_0000203 NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_provenance.
- befree-2016 importedOn "2016-02-19" NP908862.RAODOmQ2OYUvOOJKNQ6saaPgeENaIJb0UDU0kGCL3ZaYg130_provenance.