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- source_evidence_literature type ECO_0000212 NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_provenance.
- NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_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." NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_provenance.
- NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_assertion evidence source_evidence_literature NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_provenance.
- NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_assertion SIO_000772 21747397 NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_provenance.
- NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_assertion wasDerivedFrom befree-20150227 NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_provenance.
- NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_assertion wasGeneratedBy ECO_0000203 NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP919535.RASV48qQSJOvCfiObAlP1A-_bfJ0p-f7-oUH5ONddRFpg130_provenance.